5433542-1EN Rev 5

Optima PET/CT 560, 560 FX; Discovery
PET/CT 610, 710

Pre-Installation Manual
OPERATING DOCUMENTATION
5433542-1EN
Revision 5
Optima PET/CT 560, 560 FX; Discovery PET/CT 610, 710 Pre-Installation Manual
Direction 5433542-1EN, Revision 5
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Important Information
LANGUAGE
ПРЕДУПРЕЖДЕНИЕ Това упътване за работа е налично само на английски език.
(BG) • Ако доставчикът на услугата на клиента изиска друг език, задължение на
клиента е да осигури превод.
• Не използвайте оборудването, преди да сте се консултирали и разбрали

упътването за работа.
• Неспазването на това предупреждение може да доведе до нараняване на

доставчика на услугата, оператора или пациентa в резултат на токов удар,
механична или друга опасност.
警告本维修手册仅提供英文版本。
(ZH-CN) • 如果客户的维修服务人员需要非英文版本，则客户需自行提供翻译服务。
• 未详细阅读和完全理解本维修手册之前，不得进行维修。
• 忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害或其他形式的
伤害。
警告本服務手冊僅提供英文版本。
(ZH-HK) • 倘若客戶的服務供應商需要英文以外之服務手冊，客戶有責任提供翻譯服務。
• 除非已參閱本服務手冊及明白其內容，否則切勿嘗試維修設備。
• 不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性或其他的危
險。
警告本維修手冊僅有英文版。
(ZH-TW) • 若客戶的維修廠商需要英文版以外的語言，應由客戶自行提供翻譯服務。
• 請勿試圖維修本設備，除非您已查閱並瞭解本維修手冊。
• 若未留意本警告，可能導致維修廠商、操作員或病患因觸電、機械或其他危險而受
傷。
UPOZORENJE Ovaj servisni priručnik dostupan je na engleskom jeziku.

(HR) • Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan osigurati prijevod.
• Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i razumjeli ovaj
servisni priručnik.
• Zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge, operatera ili
pacijenta uslijed strujnog udara, mehaničkih ili drugih rizika.
Important Information 5
VÝSTRAHA Tento provozní návod existuje pouze v anglickém jazyce.

(CS) • V případě, že externí služba zákazníkům potřebuje návod v jiném jazyce, je zajiště‐
ní překladu do odpovídajícího jazyka úkolem zákazníka.
• Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento provozní návod a
pochopili jeho obsah.
• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního

servisu, obslužného personálu nebo pacientů vlivem elektrického proudu, respektive
vlivem mechanických či jiných rizik.
ADVARSEL Denne servicemanual findes kun på engelsk.

(DA) • Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det kundens
ansvar at sørge for oversættelse.
• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.
• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk

stød, mekanisk eller anden fare for teknikeren, operatøren eller patienten.
WAARSCHUWING Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.

(NL) • Als het onderhoudspersoneel een andere taal vereist, dan is de klant verantwoorde‐
lijk voor de vertaling ervan.
• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding

werd geraadpleegd en begrepen is.
• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de

operator of een patiënt gewond kunnen raken als gevolg van een elektrische schok,
mechanische of andere gevaren.
WARNING This service manual is available in English only.

(EN) • If a customer's service provider requires a language other than English, it is the cus‐
tomer's responsibility to provide translation services.
• Do not attempt to service the equipment unless this service manual has been con‐
sulted and is understood.
• Failure to heed this warning may result in injury to the service provider, operator or
patient from electric shock, mechanical or other hazards.
HOIATUS See teenindusjuhend on saadaval ainult inglise keeles.

(ET) • Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas keeles, vastu‐
tab klient tõlketeenuse osutamise eest.
• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga

tutvumist ja sellest aru saamist.
• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või pat‐

siendi vigastamist elektrilöögi, mehaanilise või muu ohu tagajärjel.
6 Important Information
VAROITUS Tämä huolto-ohje on saatavilla vain englanniksi.

(FI) • Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä materiaalia, tar‐
vittavan käännöksen hankkiminen on asiakkaan vastuulla.
• Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja ymmärtänyt tämän
huolto-ohjeen.
• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteis‐

ton käyttäjän tai potilaan vahingoittuminen sähköiskun, mekaanisen vian tai muun
vaaratilanteen vuoksi.
ATTENTION Ce manuel d’installation et de maintenance est disponible uniquement en anglais.

(FR) • Si le technicien d'un client a besoin de ce manuel dans une langue autre que l'an‐
glais, il incombe au client de le faire traduire.
• Ne pas tenter d'intervenir sur les équipements tant que ce manuel d’installation et
de maintenance n'a pas été consulté et compris.
• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur

ou le patient des blessures dues à des dangers électriques, mécaniques ou autres.
WARNUNG Diese Serviceanleitung existiert nur in englischer Sprache.

(DE) • Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es Aufgabe des
Kunden für eine entsprechende Übersetzung zu sorgen.
• Versuchen Sie nicht diese Anlage zu warten, ohne diese Serviceanleitung gelesen
und verstanden zu haben.
• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendienst‐

technikers, des Bedieners oder des Patienten durch Stromschläge, mechanische
oder sonstige Gefahren kommen.
ΠΡΟΕΙΔΟΠΟΙΗΣΗ Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.

(EL) • Εάν ο τεχνικός σέρβις ενός πελάτη απαιτεί το παρόν εγχειρίδιο σε γλώσσα εκτός των
αγγλικών, αποτελεί ευθύνη του πελάτη να παρέχει τις υπηρεσίες μετάφρασης.
• Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν έχετε
συμβουλευτεί και κατανοήσει το παρόν εγχειρίδιο σέρβις.
• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός

στον τεχνικό σέρβις, στο χειριστή ή στον ασθενή από ηλεκτροπληξία, μηχανικούς ή
άλλους κινδύνους.
FIGYELMEZTETÉS Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.

(HU) • Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő felelőssége
a fordítás elkészíttetése.
• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben

leírtakat nem értelmezték.
• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg

áramütés, mechanikai vagy egyéb veszélyhelyzet miatti sérülését eredményezheti.
AÐVÖRUN Þessi þjónustuhandbók er aðeins fáanleg á ensku.

(IS) • Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en ensku, er það
skylda viðskiptamanns að skaffa tungumálaþjónustu.
• Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur verið skoðuð
og skilin.
• Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda, stjórnanda
eða sjúklings frá raflosti, vélrænu eða öðrum áhættum.
AVVERTENZA Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.

(IT) • Se un addetto alla manutenzione richiede il manuale in una lingua diversa, il cliente
è tenuto a provvedere direttamente alla traduzione.
• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il pre‐

sente manuale ed averne compreso il contenuto.
• Il mancato rispetto della presente avvertenza potrebbe causare lesioni all'addetto al‐
la manutenzione, all'operatore o ai pazienti provocate da scosse elettriche, urti mec‐
canici o altri rischi.
警告このサービスマニュアルには英語版しかありません。
(JA) • サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業
者の責任で行うものとさせていただきます。
• このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでくださ
い。
• この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、
感電や機械的又はその他の危険により負傷する可能性があります。
경고 본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다.

(KO) • 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우, 번역 서비스를 제공하는
것은 고객의 책임입니다.
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지

마십시오.
• 본 경고 사항에 유의하지 않으면 전기 쇼크, 기계적 위험, 또는 기타 위험으로 인해 서

비스 제공자, 사용자 또는 환자에게 부상을 입힐 수 있습니다.
BRĪDINĀJUMS Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.

(LV) • Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā, klienta pienā‐
kums ir nodrošināt tulkojumu.
• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un sapraša‐

nas.
• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, me‐

hānisku vai citu faktoru izraisītu traumu risks apkopes sniedzējam, operatoram vai
pacientam.
ĮSPĖJIMAS Šis eksploatavimo vadovas yra tik anglų kalba.

(LT) • Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų, suteikti vertimo
paslaugas privalo klientas.
• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio

eksploatavimo vadovo.
• Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar paciento suža‐
lojimai dėl elektros šoko, mechaninių ar kitų pavojų.
ADVARSEL Denne servicehåndboken finnes bare på engelsk.

(NO) • Hvis kundens serviceleverandør har bruk for et annet språk, er det kundens ansvar
å sørge for oversettelse.
• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.
• Manglende hensyn til denne advarselen kan føre til at serviceleverandøren, oper‐
atøren eller pasienten skades på grunn av elektrisk støt, mekaniske eller andre
farer.
OSTRZEŻENIE Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.

(PL) • Jeśli serwisant klienta wymaga języka innego niż angielski, zapewnienie usługi tłu‐
maczenia jest obowiązkiem klienta.
• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręczni‐

kiem serwisowym i zrozumienia go.
• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisan‐

ta, operatora lub pacjenta w wyniku porażenia prądem elektrycznym, zagrożenia
mechanicznego bądź innego.
ATENÇÃO Este manual de assistência técnica encontra-se disponível unicamente em inglês.

(PT-BR) • Se outro serviço de assistência técnica solicitar a tradução deste manual, caberá ao
cliente fornecer os serviços de tradução.
• Não tente reparar o equipamento sem ter consultado e compreendido este manual
de assistência técnica.
• A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou

paciente decorrentes de choques elétricos, mecânicos ou outros.
ATENÇÃO Este manual de assistência técnica só se encontra disponível em inglês.

(PT-PT) • Se qualquer outro serviço de assistência técnica solicitar este manual noutro idio‐
ma, é da responsabilidade do cliente fornecer os serviços de tradução.
• Não tente reparar o equipamento sem ter consultado e compreendido este manual
de assistência técnica.
• O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do

operador ou do paciente devido a choques eléctricos, mecânicos ou outros.
ATENŢIE Acest manual de service este disponibil doar în limba engleză.

(RO) • Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât cea engleză,
este de datoria clientului să furnizeze o traducere.
• Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui

manual de service.
• Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului

sau pacientului în urma pericolelor de electrocutare, mecanice sau de altă natură.
ОСТОРОЖНО! Данное руководство по техническому обслуживанию представлено только на

(RU) английском языке.
• Если сервисному персоналу клиента необходимо руководство не на
английском, а на каком-то другом языке, клиенту следует самостоятельно
обеспечить перевод.
• Перед техническим обслуживанием оборудования обязательно обратитесь к

данному руководству и поймите изложенные в нем сведения.
• Несоблюдение требований данного предупреждения может привести к тому,

что специалист по техобслуживанию, оператор или пациент получит удар
электрическим током, механическую травму или другое повреждение.
UPOZORENJE Ovo servisno uputstvo je dostupno samo na engleskom jeziku.

(SR) • Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da obezbedi prevodi‐
lačke usluge.
• Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo servisno uputst‐
vo.
• Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca

ili pacijenta usled strujnog udara ili mehaničkih i drugih opasnosti.
UPOZORNENIE Tento návod na obsluhu je k dispozícii len v angličtine.

(SK) • Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu, poskytnutie
prekladateľských služieb je zodpovednosťou zákazníka.
• Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a nepor‐

ozumiete mu.
• Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, ob‐

sluhujúcej osoby alebo pacienta elektrickým prúdom, mechanické alebo iné ohroze‐
nie.
ATENCION Este manual de servicio sólo existe en inglés.

(ES) • Si el encargado de mantenimiento de un cliente necesita un idioma que no sea el
inglés, el cliente deberá encargarse de la traducción del manual.
• No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido

este manual de servicio.
• La no observancia del presente aviso puede dar lugar a que el proveedor de servi‐
cios, el operador o el paciente sufran lesiones provocadas por causas eléctricas,
mecánicas o de otra naturaleza.
VARNING Den här servicehandboken finns bara tillgänglig på engelska.

(SV) • Om en kunds servicetekniker har behov av ett annat språk än engelska, ansvarar
kunden för att tillhandahålla översättningstjänster.
• Försök inte utföra service på utrustningen om du inte har läst och förstår den här
servicehandboken.
• Om du inte tar hänsyn till den här varningen kan det resultera i skador på servicete‐
knikern, operatören eller patienten till följd av elektriska stötar, mekaniska faror eller
andra faror.
OPOZORILO Ta servisni priročnik je na voljo samo v angleškem jeziku.

(SL) • Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora stranka za‐
gotoviti prevod.
• Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razu‐

meli.
• Če tega opozorila ne upoštevate, se lahko zaradi električnega udara, mehanskih ali

drugih nevarnosti poškoduje ponudnik storitev, operater ali bolnik.
DİKKAT Bu servis kılavuzunun sadece ingilizcesi mevcuttur.

(TR) • Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan talep
ederse, bunu tercüme ettirmek müşteriye düşer.
• Servis kılavuzunu okuyup anlamadan ekipmanlara müdahale etmeyiniz.
• Bu uyarıya uyulmaması, elektrik, mekanik veya diğer tehlikelerden dolayı teknisyen,

operatör veya hastanın yaralanmasına yol açabilir.
Revision History
Revision Date Reason for Change
5 4-May-2017 Updated for PARC4 (Q.Core Power) upgrade option. Chapter 1: Updated Table 1-2 to add
PARC4 (Q.Core Power) size and weight dimensions and revise dolly width and length dimen‐
sions per Engineering. Added section 4.2.2.6 for PARC4 (Q.Core Power) shipping methods. Up‐
dated section 4.4.4 for unpacking PARC4 (Q.Core Power). Chapter 2: Updated Table 2-1 to add
PARC4 (Q.Core Power) system component weight load. Updated Table 2-2 for PARC4 (Q.Core
Power) system component dimensions. Added Illustration 2-4 and table below for PARC4
(Q.Core Power) dimensions. Added Illustration 2-13 and table below for PARC 4 center-of-gravi‐
ty. Updated table below Illustration 2-16 typical scan suite layout for PARC4 (Q.Core Power).
Added section 3.8 for PARC4 (Q.Core Power) placement requirements. Updated section 4.1.1
for PARC4 (Q.Core Power) non-seismic anchoring statement. Chapter 4: Updated section 1.1.2
for Q.Core/PARC4 (Q.Core Power). Renamed section 1.2 from “System Cooling Requirements”
to “Heat Output” to match other products. Added heat output text for PARC4 (Q.Core Power).
Updated Table 4-3 with PARC4 (Q.Core Power) heat output. Updated Table 4-3 with Q.Core
(Recon Cabinet) heat output.Chapter 5: Updated sections 1.4.4 and 1.9 for Continuous (average)
power demand at maximum duty cycle value. Updated table below Illustration 5-2 system ground
map for PARC4 (Q.Core Power). Updated Table 5-8 for PARC4 (Q.Core Power) component des‐
ignators. Updated text in section 3.1 for PARC4 (Q.Core Power) upgrade cable kits. Added Table
5-17 and 5-18 for PARC4 (Q.Core Power) upgrade cable kits.
4 9-Oct-2014 HCSDM00314963: Chapter 5: Updated section 3.1 for new cable catalogs P5051TE, P5051TF,
P5064TE, and P5064TF.
3 24-May-2013 HCSDM00196987: Chapter 1: Updated section 4.1.1. Table 1-2: Corrected width for PET Image
Ring with dollies and PET Source Ring/Trailer with dollies. Updated Illus 1-3 and 1-4. Chapter 2:
Corrected weights for Console, Monitor, and Workspace Table in Table 2-1. Corrected height for
Q.Core and Operator Console in Table 2-2, Illus 2-3, and Illus 2-11. Corrected weights for Illus
2-4, and Illus 2-6 through 2-9.
2 26-Mar-2013 Front/back cover updates. HCSDM00179998: Chapter 1, section 2: Corrected “Floor Specifica‐
tion” minimum concrete thickness; Table 1-2: Weights corrected for CT Gantry (16 slice) and PET
Image Ring. Chapter 2, Table 2-1: Weights corrected for CT Gantry (16 slice), Patient Table, and
PDU; section 3: Removed VQC phantom from Tables 2-5 and 2-6. Chapter 3: Added section
1.2.6 – PET Alignment (VQC) Phantom. Chapter 5, Tables 2-9 and 2-10: Corrected cable length
for Run # 56. Entire manual: Moved descriptive text in illustrations to tables.
1 8-Aug-2012 Initial release.
Revision History 13
14 Revision History
Table of Contents
Chapter 1 GENERAL REQUIREMENTS............................................................................................... 23
1 Introduction....................................................................................................................................23
1.1 Objective and Scope of this Manual..................................................................................... 23
1.2 Responsibility of the Customer.............................................................................................23
1.3 Site Project Coordinator....................................................................................................... 24
2 System Siting Requirements......................................................................................................... 25
2.1 Project Manager (PM) Tasks................................................................................................25
2.2 Customer Requirements for Site Readiness........................................................................ 25
3 Regulatory Requirements..............................................................................................................30
3.1 Building Codes, Regulations and Permits............................................................................ 30
3.2 Clearance Regulations......................................................................................................... 30
3.3 Codes, Clearances, and Service Space Regulation.............................................................30
4 Delivery and Handling................................................................................................................... 31
4.1 Project Manager Tasks.........................................................................................................31
4.1.1 Minimum Doorway Opening........................................................................................ 31
4.1.2 Minimum Hallway Width.............................................................................................. 31
4.2 Shipping Dimensions and Weight.........................................................................................31
4.2.1 Delivery Sizes and Weights......................................................................................... 31
4.2.2 Shipping Methods (Dollies, Skids)............................................................................... 32
4.2.2.1 CT Gantry........................................................................................................... 32
4.2.2.2 PET Components............................................................................................... 33
4.2.2.3 Patient Table.......................................................................................................34
4.2.2.4 PDU.................................................................................................................... 35
4.2.2.5 Q.Core................................................................................................................ 35
4.2.2.6 PARC4 (Q.Core Power) Reconstruction Cabinet............................................... 35
4.2.2.7 Operator Console............................................................................................... 36
4.3 System Lifting and Rigging Restrictions............................................................................... 36
4.4 Shipping and Receiving........................................................................................................36
4.4.1 Handling Restrictions...................................................................................................36
Table of Contents 15
4.4.2 Dollies.......................................................................................................................... 37
4.4.3 Delivery Temperature and Humidity Tolerance........................................................... 37
4.4.4 Unpacking System.......................................................................................................37
4.5 Storage................................................................................................................................. 38
Chapter 2 EQUIPMENT REQUIREMENTS........................................................................................... 39

1 System Components..................................................................................................................... 39
1.1 Component Weight/Load, Dimensions, and Center of Gravity.............................................39
1.2 System Component Diagrams..............................................................................................40
1.3 System Component Center-of-Gravity Diagrams................................................................. 44
2 Room Layout................................................................................................................................. 51
2.1 Scan Suite Configuration......................................................................................................51
2.2 Minimum Scan Room Sizing................................................................................................ 52
2.2.1 Scan Room Operational Space Requirement..............................................................52
2.2.2 Scan Room Equipment Accessibility........................................................................... 53
2.3 Minimum Control Room Sizing............................................................................................. 53
2.3.1 Control Room Considerations and Requirements....................................................... 53
2.3.2 Autoinjector Control Placement................................................................................... 53
2.4 Control Room Scanner Desktop Requirements................................................................... 53
2.4.1 Scanner Desktop Configuration...................................................................................53
2.4.2 Scanner Desktop Clearance........................................................................................53
2.4.3 Scanner Desktop Power.............................................................................................. 53
2.4.4 Scanner Desktop Cables............................................................................................. 53
3 Hospital Equipment and Service Space Requirements.................................................................54
3.1 Clearances........................................................................................................................... 54
3.1.1 Operational Clearances............................................................................................... 54
3.1.2 Emergency Medical Equipment Clearances................................................................54
3.1.3 Replacement Parts and Service Equipment Space.....................................................54
3.1.4 Ceiling Height Requirements....................................................................................... 54
3.2 Workplace Requirements..................................................................................................... 54
3.2.1 U.S. Code Requirements.............................................................................................54
16 Table of Contents
3.2.2 Cover Removal Clearance...........................................................................................58

3.3 Cover Clearance Requirements........................................................................................... 58
3.3.1 Gantry Front Cover – Removal Clearance...................................................................58
3.3.2 Gantry Front Cover – Service Clearance.....................................................................58
3.3.3 Gantry Rear Cover – Removal Clearance................................................................... 58
3.4 Gantry Space Requirements................................................................................................ 58
3.5 PDU Placement Requirements.............................................................................................59
3.6 Scanner Desktop Placement Requirements.........................................................................59
3.6.1 Scanner Desktop Depth...............................................................................................59
3.6.2 Scanner Desktop Operating Space............................................................................. 59
3.7 Q.Core Placement Requirements.........................................................................................59
3.8 PARC4 (Q.Core Power) Reconstruction Cabinet Placement Requirements........................60
3.9 Trailer Requirements............................................................................................................ 60
3.10 Storage Cabinet Requirements.......................................................................................... 60
3.11 Verify Site Print...................................................................................................................61
4 Anchoring...................................................................................................................................... 62
4.1 Anchoring Requirements – Non-Seismic Installation............................................................62
4.1.1 Gantry, Patient Table, and Trailer Anchoring – Non-Seismic...................................... 62
4.1.2 GE-Supplied Anchors.................................................................................................. 63
4.1.3 Anchor Placement....................................................................................................... 64
4.1.4 Minimum Number of Anchors...................................................................................... 64
4.2 Anchoring Requirements – Seismic Installation................................................................... 64
Chapter 3 SPECIAL CONSTRUCTION REQUIREMENTS................................................................... 65

1 Radiation Protection...................................................................................................................... 65
1.1 X-Ray Radiation Protection.................................................................................................. 65
1.1.1 Shielding Requirements...............................................................................................65
1.1.2 System X-ray Scatter Envelope...................................................................................66
1.2 Gamma Ray Protection........................................................................................................ 69
1.2.1 Protection of Equipment.............................................................................................. 70
1.2.2 Protection of Personnel............................................................................................... 70
1.2.3 Barriers, Partitions and Shielding................................................................................ 70

1.2.4 External Sources of Radiation..................................................................................... 71
1.2.5 Dose Rate from Radioactive Pin Source..................................................................... 71
1.2.5.1 Dose Rates with Pin Source Stored................................................................... 72
1.2.5.2 Dose Rates with Pin Source in Use....................................................................72
1.2.6 PET Alignment (VQC) Phantom.................................................................................. 73
2 Electromagnetic Interference (EMI) Consideration....................................................................... 74
2.1 Electromagnetic Interference (EMI) System Placement.......................................................74
2.1.1 EMI – Gantry................................................................................................................74
2.1.2 EMI – PDU................................................................................................................... 74
2.1.3 EMI – Scanner Desktop/Computer Equipment............................................................ 74
2.1.4 Electromagnetic Immunity........................................................................................... 74
2.1.5 Electromagnetic Separation Distance..........................................................................75
2.1.6 Cable Shielding and Grounding...................................................................................76
2.2 Electromagnetic Emission.................................................................................................... 76
3 Vibration Isolation..........................................................................................................................78
3.1 Scanning Facility Vibration Isolation.....................................................................................78
3.2 Frequency/Vibration Range..................................................................................................78
4 Other Construction Considerations............................................................................................... 81
4.1 Patient Viewing Window Dimensions................................................................................... 81
4.2 Support Structure Installation............................................................................................... 81
4.3 Chemical Contamination Concerns...................................................................................... 81
4.4 Finished Wall Requirement.................................................................................................. 81
4.4.1 Wall Paint.....................................................................................................................81
4.4.2 Wall Paint - Exception..................................................................................................81
4.5 Option Requirements............................................................................................................81
4.5.1 Non-GE Installed Options............................................................................................ 81
4.5.2 GE Options.................................................................................................................. 81
4.5.3 Options Power and Control Cables............................................................................. 82
Chapter 4 ENVIRONMENTAL REQUIREMENTS (HVAC).................................................................... 83

1 HVAC Requirements..................................................................................................................... 83
1.1 Climate Requirements.......................................................................................................... 83
1.1.1 Air Quality.................................................................................................................... 83
1.1.1.1 Construction Dust Concerns...............................................................................83
1.1.1.2 Chemical Contamination Concerns.................................................................... 83
1.1.2 Temperature and Humidity Requirements...................................................................83
1.1.3 Altitude Operating Range............................................................................................ 84
1.1.4 Environmental Conditions Verification......................................................................... 84
1.1.5 Patient Comfort............................................................................................................84
1.2 Heat Output.......................................................................................................................... 84
1.3 Air-Handling System Initial Start-Up Considerations............................................................ 85
Chapter 5 ELECTRICAL REQUIREMENTS.......................................................................................... 87

1 Power Requirements.....................................................................................................................87
1.1 Regulations...........................................................................................................................87
1.2 Disconnects.......................................................................................................................... 87
1.2.1 Emergency Off Switch................................................................................................. 87
1.2.2 Local Disconnects........................................................................................................87
1.3 Electrical and Junction Boxes...............................................................................................88
1.4 Power Feed and Overcurrent Requirements........................................................................88
1.4.1 Power Feed................................................................................................................. 88
1.4.2 Voltage.........................................................................................................................88
1.4.3 Frequency....................................................................................................................88
1.4.4 Average Power Demand at Maximum Duty Cycle.......................................................88
1.4.5 Maximum Power Demand........................................................................................... 88
1.4.6 Under voltage Release Control....................................................................................88
1.4.7 Overcurrent Protection.................................................................................................88
1.4.8 Voltage Regulation Effects.......................................................................................... 88
1.4.9 Load Regulation...........................................................................................................89
1.5 Phase Imbalance..................................................................................................................89
1.6 Sags, Surges, and Transients.............................................................................................. 89

1.6.1 Sags and Surges......................................................................................................... 89
1.6.2 Transient Voltage.........................................................................................................89
1.7 Power Source Configuration.................................................................................................89
1.7.1 Neutral Wire.................................................................................................................89
1.7.2 Dedicated Feeder........................................................................................................ 89
1.7.3 Protective Disconnect Device Location....................................................................... 89
1.7.4 Protective Disconnect Device with LOCK-OUT/TAG-OUT .........................................89
1.8 Dedicated Distribution Transformer......................................................................................89
1.8.1 Dedicated Feeder........................................................................................................ 89
1.8.2 Power Distribution Transformer................................................................................... 89
1.8.3 Using an Existing Distribution Transformer................................................................. 90
1.9 System Power Requirements (64 Slice Discovery 610, Discovery 710).............................. 90
1.10 System Power Requirements (16 Slice Optima 560, Discovery 610, Discovery 710)........91
2 Grounding......................................................................................................................................93
3 System Interconnection and Cabling.............................................................................................95
3.1 Component Interconnections................................................................................................95
3.1.1 Component Designators.............................................................................................. 95
3.1.2 Cable Specifications.................................................................................................... 96
3.2 Cable Routing Requirements............................................................................................. 103
3.2.1 Properly Sized Conduit, Duct Work, and Floor Troughs............................................103
3.2.2 Future Expansion.......................................................................................................103
3.2.3 Routing Power Wiring................................................................................................ 103
3.2.4 Power and System Control Wire Separation............................................................. 103
4 Scan Room Warning Light and Door Interlock............................................................................ 104
4.1 X-Ray Warning Light.......................................................................................................... 104
4.2 Scan Room Door Interlock Connections............................................................................ 104
Chapter 6 COMMUNICATIONS REQUIREMENTS............................................................................. 107

1 Network Requirements................................................................................................................107
1.1 Communication Network.................................................................................................... 107
1.1.1 Network Wall Outlet................................................................................................... 107

1.1.2 Network Speed.......................................................................................................... 107
1.1.3 Network Communication............................................................................................107
1.1.4 Patch Cable............................................................................................................... 107
1.1.5 Cable Duct Work........................................................................................................107
1.1.6 Communication Run to RJ45 Wall Outlet.................................................................. 107
1.2 Zone Broadband Specialist................................................................................................ 107
1.2.1 Contact GE PM..........................................................................................................107
1.2.2 IT Infrastructure Changes.......................................................................................... 107
1.2.3 IP Addresses............................................................................................................. 107
1.2.4 VPN Compatible Appliance....................................................................................... 107
1.2.5 Internet Service Provider........................................................................................... 107
1.3 IT Site Contact Information.................................................................................................108
1.3.1 GE PM Information.................................................................................................... 108
1.3.2 Coordinate VPN Activities..........................................................................................108
1.3.3 Ensuring Broadband Infrastructure Requirements.................................................... 108
1.3.4 Equipment Assessment............................................................................................. 108
Chapter 1 General Requirements

1 Introduction
1.1 Objective and Scope of this Manual
This manual is the official guide and informational resource for planning and preparing a
location for the installation of the following PET/CT systems. The responsibility of arranging and
paying for all work associated with site planning, site preparation, and system installation rests
solely with the buyer/purchaser of the system.
• Optima™ PET/CT 560
• Optima™ PET/CT 560 FX
• Discovery™ PET/CT 610
• Discovery™ PET/CT 710
This manual guides you through the pre-installation siting and regulatory requirements. Keep in
mind, this manual cannot address or answer each and every site specific question or concern.
Contact your GE Healthcare Project Manager (PM) for answers to any additional questions or
concerns not addressed in this manual. Prior to any construction or approval, General Electric
Headquarters Architectural Planning must review all PET/CT preliminary concepts, site plans,
and final working drawings associated with the installation of the system. Contact your GE PM
or complete information regarding your site-specific room layout.
1.2 Responsibility of the Customer
It is the responsibility of the customer (buyer/purchaser) to prepare the site in accordance with
all the specifications provided in this manual and in conjunction with site-specific drawings and
applicable regulations. It is essential to verify all aspects of the site configuration before
construction has begun, as subsequent changes can be costly or impractical. A detailed pre-
installation checklist is provided in this manual. It is the responsibility of the customer to ensure
all requirements on the checklist are fulfilled and that the site conforms to all specifications and
requirements detailed in this manual.
Pre-Installation requirements shall include the procurement and installation of all required
materials and services necessary to prepare the room to be ready for installation of the PET/CT
system. The customer is responsible for all aspects of site preparation, including:
• Assigning a project coordinator.
• Planning and construction requirements for the installation of the PET/CT system in
accordance with all national, state, or local regulatory requirements for the country in which
the installation occurs, for example:
○ Fire control devices as required by local codes.

○ Permits, inspections, radiation licensing, etc.
○ Earthquake-related regulations.
• Selecting a location suitable for the installation of the PET/CT system.
Chapter 1 General Requirements 23

• Constructing or renovating the site.
• All design work associated with preparing the installation site for the PET/CT system and all
architectural, mechanical, and electrical drawings associated with the design of the site.
• All alterations or modifications to products not specifically included in the sales contract.
• A clean and safe work environment for installation of the PET/CT system.
• A location with proper lighting, a level finished floor, finished walls, and a finished ceiling.
• A support structure in the floor, walls, and ceiling suitable for mounting all system
components as specified in the site design.
• Installation of all required conduit, ducts, and raceways to safely route all cables.
• Supplying electrical power of the required voltage, all necessary power supply cables and
grounds, all necessary power cables and grounds to the PDU and system cabinet, and an
Emergency-Off switch in the scan room.
• Installation of all properly-sized junction boxes, outlets with covers, line safety switches, and
fittings installed at the locations specified in the site design.
• All Non-GE wires and cables as specified in this document:
○ The electrical contractor shall ring out and tag all wires at both ends.
○ Wires shall be continuous and without splices.
○ Ground wires shall conform to product requirements.
○ Color-coded wires shall be used whenever possible, to enable easier identification.
• All work shall conform to IBC (International Building Code) and local building and safety
codes.
NOTE: GE Healthcare does not provide or install the wires, conduits, junction boxes, or
ducting illustrated in this publication, unless specifically stated.
1.3 Site Project Coordinator
The site project coordinator is the primary contact and liaison between GE Healthcare and all
site related functions, between the purchaser, the construction planners, architects, contractors,
and any other site administrative personnel.
To ensure a successful installation, it is recommended that a single/individual site project
coordinator manage the entire project. Ideally, the project coordinator is a person familiar with
all phases of pre-installation and installation of similar medical device construction projects, from
conceptual planning through to system start up. The site project coordinator shall be responsible
for working closely with GE Healthcare to ensure the client (buyer/purchaser) upholds all
requirements in this manual.
24 1 Introduction
2 System Siting Requirements

• System Site Print
A system installation, relocation, or move requires a site print. The PET/CT room layout shall
match the layout detailed on the site print.
• Regulatory Code & System Requirements

A site shall meet all regulatory code and system requirements associated with; service,
structural, flooring, vibration, HVAC, electrical, IT network, radiation protection, operational
clearance requirements, and all applicable codes.
• Floor Specification
The floor shall have a minimum concrete thickness of 127 mm (5 in.).
The floor shall be no greater than 6 mm (0.250 in.) out of level over a 3048 mm (10 ft.)
range, with level defined as the horizontal surface between the highest and lowest points.
NOTE: If the concrete floor has a floor covering installed over it (such as floor tile), 17 or
more openings 101.6 mm (4 in.) in diameter will be cut into the floor covering to
ensure the table and gantry rest on the concrete. (Openings are cut during
installation.)
Shims shall not be used to level the gantry or patient table.
• Related Hospital Equipment Clearances

Carefully check/verify the room layout for the necessary clearances required of any related
hospital equipment. Good judgment is required to avoid compromising important system
features. There shall be ample maneuvering space around the patient table for a hospital
cart, any emergency equipment, and all personnel, etc.
2.1 Project Manager (PM) Tasks

GE Healthcare Project Manager (PM) will assist buyer with system siting requirements.
2.2 Customer Requirements for Site Readiness
• Site Readiness Completion and Verification
Installation cannot proceed until all site-readiness requirements have been completed and
verified. A site is ready when all renovations/modifications have been completed and the
scan suite meets all regulatory, code, and system requirements, system delivery needs, and
all requirements for any options.
• Contractor’s Final Confirmation

Final confirmation of installation site readiness shall be made by all contractors associated
with the project; structural engineer/architect, HVAC contractor, electrical contractor,
qualified radiological health physicist, cleaning service, etc.
• Schedule of Site-Ready Visit

To ensure timely system delivery and installation, the customer shall complete all necessary
work listed in this Pre-Installation Manual and schedule a site-ready Project Manager (PM)
visit prior to system delivery.
• Pre-installation Checklist
The customer shall also verify site readiness by filling out and signing the following Pre-
Installation Checklist. The checklist shall be completed six weeks prior to scheduled delivery
date.
Table 1-1: Customer Pre-Installation Checklist - Required Information for Site
Complete prior to scheduled delivery date.

Today's Date:
Hospital Name:
(as it appears on the system screen)
Network ID numbers/IP Addresses: List IP Numbers and Address
AW
AW Direct Connect Address:
Camera
Camera Setup Information
PACS
Other ___________________________
Other ___________________________
Do you want HIPAA enabled? Yes No
Do you want automatic downloads enabled? Yes No
Commitment Dates:
Action Item Completed?

Action Item Comments
Yes No
Have the facilities department, contractor, and GE

Healthcare certified the project schedule?
Will committed site-ready date be met?
Does construction completion date meet or precede

the delivery date?
Is the Power & Ground survey complete?

Hospital Contact Name/No.
___________________________
___________________________
Is the site-ready visit scheduled?
Is the delivery date scheduled?
Does the delivery date require adjustment?
Is the installation date scheduled?
26 2 System Siting Requirements

Does the installation date require adjustment?
Is the installation timing determined?
Weekdays
Weekend
Quick Install
If Weekend or Quick Install selected, have all sub-

contractors been notified?
Is the system first-use date scheduled?
Are system applications/training dates scheduled?
On-Site Training Date:

________________________
Healthcare Institute Training Date:

_______________________
Equipment Compatibility:

Yes No
Has the order been reviewed for completeness and

compatibility with existing equipment?
Remote Monitors
AW Relocation
Cardiac Option
Injectors
Are interfaces to existing or new accessories ordered

and planned accordingly?
Are cables of the correct length on order?
Have the locations of the following peripherals (or op‐

tions) been included in the site drawings?
EKG Monitor
Injector Control
Laser camera
UPS
2nd Monitor
Respiratory Gating
Site Planning Requirements:

Yes No

Were final drawings approved and distributed to the

contractors?
Are final drawings signed off to approve equipment

layout and orientation?
Has the surface penetration permit been obtained and

signed?
Do the actual room dimensions match those on the fi‐

nal drawings?
Has VQC Phantom been ordered by customer?
Is RAM license valid?
Is Radiation Safety Officer ready to receive Pin

Source and VQC Phantom?
Has the radiologist health physician reviewed and ap‐

proved the room layout shielding requirements?
Have any additional requirements or questions about List additional items:

the installation been discussed with GE Healthcare?
Is there a person assigned to review and verify that all

installation requirements are met?
Have the specific site requirements been discussed

with all contractors?
Has the responsibility of cabling, installing, and inter‐

facing any GE approved accessories not on the order
been discussed with GE Healthcare?
Are all third-party vendors identified, notified, and

scheduled?
Have all Regulatory, Code, & System Requirements

been met?
Has it been verified there is no plumbing or any

grounded surface within 1.83 m (6 ft.) of the table or
gantry?
Will the existing network, broadband, and camera ca‐ List any issues or concerns:
ble drops reach all required locations for the PET/CT
scanner?
Network Installation:

Yes No
Have IP address and host names been obtained?
Will a network camera be used?
Required: Is the network installed, are the network

jacks installed, and is the entire network tested?
Required: Is the broadband VPN installed and setup?
Required: Are network software options ordered?
HIS RIS Option
DICOM Print
AW
28 2 System Siting Requirements

Delivery and Miscellaneous:

Yes No
Have arrangements been made in the schedule to al‐

low adequate time for remodeling, if required (such as
construction, floor or ceiling work, painting, or other
cosmetic work)?
Have arrangements been made to clean the floor af‐

ter equipment removal and prior to the installation of
the new equipment?
Is de-installation of existing equipment required?
Is there a trade-in of existing equipment?
GoldSeal
Has the delivery route been identified with the proper

hospital personnel?
Have the elevators and doors been checked for size

and weight constraints?
Have the appropriate arrangements been made with

traffic for delivery?
Will any acceptance, performance, or bio-medical

testing be required?
Are trash and recycling bins available for the disposal

of paper, cardboard, etc.

3 Regulatory Requirements
The following codes, standards, and laws are referenced in this section:
• OSHA 29 CFR 1910
• NFPA 70E (Standard for Electrical Safety in the Workplace)
• NFPA 101: (Life Safety Code)
• NFPA 99: (Standard for Health Care Facilities)
• ADA Amendments Act of 2008 (Americans with Disabilities Act)
3.1 Building Codes, Regulations and Permits

Building Codes and Regulations Scan suite shall meet all building codes and applicable
regulations.
GE Healthcare Surface Penetration Permit A GE surface penetration permit shall be approved
by the appropriate facility or building representative. (Drilling holes into a concrete floor is an
example of surface penetration.) The GE surface penetration permit can be obtained through
GE Healthcare Service Operations, EHS Support Central.
3.2 Clearance Regulations
Federal & National Association Regulations
Clearance regulations for all systems installed in the U.S. are determined by various federal
agencies and the National Fire Protection Association. The regulating publications are: OSHA
29 CFR 1910, NFPA 70E (Standard for Electrical Safety in the Workplace), NFPA 101: (Life
Safety Code), NFPA 99: (Standard for Health Care Facilities), and the ADA Amendments Act of
2008 (Americans with Disabilities Act).
Federal and Foreign Regulations
All systems installed within the U.S. and its territories shall comply with all federal and local
regulations. Systems installed outside the U.S. shall comply with either the national state or
local regulatory clearance requirements for the country in which the installation occurs, or U.S.
federal regulations, whichever is greater.
3.3 Codes, Clearances, and Service Space Regulation
Federal, State, and Local Codes The diagrams and dimensions used throughout this manual,
detail required clearances for proper system operation and servicing only. The customer shall
be responsible for ensuring all federal, state, and local codes and clearances are followed and
maintained, regarding facility egress and all other related requirements.
30 3 Regulatory Requirements
4 Delivery and Handling

4.1 Project Manager Tasks
Task Description
Site Dimensions PM shall measure and verify all site dimensions to ensure the facility can ac‐
commodate the delivery of the system (and any related components or
equipment), from the delivery drop-off point to the scan suite.
NOTE: The minimum unobstructed doorway opening to accommodate
delivery of the system is 1067 mm (42 in.). The minimum un‐
obstructed hallway width to accommodate delivery of the sys‐
tem is 1803 mm (71 in.).
Delivery Type PM shall determine type of delivery: ground level, loading dock, or tilt-bed
truck.
Delivery Equipment PM shall determine if delivery requires special dollies, lifting crates, or rig‐
gers. PM shall order any additional delivery equipment and all necessary de‐
livery personnel.
NOTE: The CT gantry cannot be lifted or transported by any means
other than the GE support cradle and dolly system on which is
was shipped. Otherwise, serious damage to the gantry could
result. The CT gantry is not designed to be lifted by special rig‐
ging.
Identify Delivery Route PM shall identify the delivery route, which may include any elevators, door‐
ways, and hallways necessary to accommodate the delivery of all system
components.
Non-Construction-Zone Route to Scan Suite PM shall verify an accessible, dust-free, non-construction-zone delivery
route to the scan suite.
Packaging Requirements PM shall order any construction site packaging requirements prior to ship‐
ment. Packaging cannot be modified once the system is shipped.
Floor Protection PM shall determine if floor protection is required along facility delivery route
and communicates requirement to delivery company/personnel.
4.1.1 Minimum Doorway Opening

The minimum unobstructed doorway opening to accommodate delivery of the system is 1067
mm (42 in.). This accommodates the CT Gantry with covers and dollies attached, but side rails
removed. This also accommodates the PET Image Ring with dollies attached, but side
protective braces removed.
4.1.2 Minimum Hallway Width
The minimum unobstructed hallway width to accommodate delivery of the system is 1803 mm
(71 in.).
4.2 Shipping Dimensions and Weight
4.2.1 Delivery Sizes and Weights

Table 1-2: Estimated Loading Dock Delivery Sizes and Weights
Item Height mm (in.) Width/Depth mm Length mm (in.) Weight kg (lb)

(in.)
CT Gantry (64 Slice) with Dollies On, Side Rails On 1955 (77) 1295 (51) 2438.4 (96) 1932 (4260)
CT Gantry (64 Slice) with Dollies On, Side Rails Off 1955 (77) 970 (38.25) 2438.4 (96) 1914 (4220)
CT Gantry (16 slice) with Dollies On, Side Rails On 2000 (79) 1290 (51) 2810 (111) 1982 (4360)
CT Gantry (16 slice) with Dollies On, Side Rails Off 2000 (79) 1067 (42) 2810 (111) 1967 (4310)
PET Base and Retractor Assembly with Dollies 990 (39) 1054 (41.5) 2286 (90) 678 (1495)
PET Image Ring with Dollies On, Side Protective 1880 (74) 1041.4 (41) 2667 (105) 1282 (2820)
Braces On
PET Image Ring with Dollies On, Side Protective 1880 (74) 985.52 (38.8) 2667 (105) 1282 (2820)
Braces Off
PET Image Ring without Dollies 1819 (72) 720 (28) 1931 (76) 954 (2110)
PET Image Ring Dolly (assembled) — 1041.4 (41) 2667 (105) 327 (720)
PET Source Ring and Trailer with Dollies 1092 (43) 1041.4 (41) 2387.6 (94) 608 (1340)
Table (Blue Dollies On) 1410 (55.5) 864 (34) 3836 (151) 1241 (2736)
Table (Blue Dollies Off, Red Castors On) 1410 (55.5) 1016 (40) 3048 (120) 1295 (2856)
Table (Tilting Dollies On) 1778-2032 965 (38) 2489-2921 1147 (2530)
(70-80) (98-115)
Power Distribution Unit (with cardboard packaging) 1092 (43) 584 (23) 762 (30) 413 (910)
Q.Core (on skid) 1067 (42) 635 (25) 864 (34) 87 (192)
PARC4 (Q.Core Power) Reconstruction Cabinet (on 1655 (65.2) 1480 (58.3) 980 (38.6) 304 (670)
skid)
Console (on skid) 1067 (42) 635 (25) 864 (34) 87 (192)
4.2.2 Shipping Methods (Dollies, Skids)

4.2.2.1 CT Gantry
The CT Gantry ships with the front and rear covers attached to its front and rear cover brackets.
During installation, the rear cover is transferred to the PET Gantry, and the rear cover brackets
are removed from the CT Gantry. The assembly is mounted between two dollies Illustration 1-1.
Two side rails are bolted to the dollies to stabilize dollies and protect the CT Gantry. The dolly
elevating casters lift the CT Gantry off its base and roll it into position.
32 4 Delivery and Handling

Illustration 1-1: CT Gantry with Shipping Dollies and Side Rails
4.2.2.2 PET Components

The PET Gantry consists of:
• PET Base and Retractor Assembly (see Illustration 1-2). The PET Base dollies have a
center stabilizing frame to protect the exposed components.
• PET Image Ring (see Illustration 1-3)
• PET Source Ring and Trailer (see Illustration 1-4)
Illustration 1-2: PET Base and Retractor Assembly, with Shipping Dollies

Illustration 1-3: PET Gantry Image Ring, with Shipping Dollies and Side Rails
Illustration 1-4: PET Source Ring and Trailer, with Shipping Dollies and Side Rails
4.2.2.3 Patient Table

The patient table ships to domestic (North American) installations on a set of dollies with
stabilizing side rails (see Illustration 1-5). The secondary base covers ship separately.

Red caster towers ship attached to the ends of the dollies (see Illustration 1-5). They are used
for fitting the Table in an elevator and for final positioning of the Table in front of the Gantry (see
Illustration 1-6).
NOTE: The patient table ships to international sites in a crate. The installation team uncrates
the table and attaches the dollies at the site.
Illustration 1-5: Patient Table with Shipping Dollies
Illustration 1-6: Patient Table on Red Caster Towers
4.2.2.4 PDU
The PDU is shipped on a skid. Do not remove the PDU from the skid until it is in the room ready
for installation.
4.2.2.5 Q.Core
The Q.Core is shipped on a skid. Do not remove the Q.Core from the skid until it is in the room
ready for installation.
4.2.2.6 PARC4 (Q.Core Power) Reconstruction Cabinet
The PARC4 (Q.Core Power) is shipped on a skid. Do not remove the PARC4 (Q.Core Power)
from the skid until it is in the room ready for installation.

Illustration 1-7: PARC4 (Q.Core Power) Packaging
4.2.2.7 Operator Console

The Console is shipped on a skid. Do not remove the Console from the skid until it is in the
equipment room. The keyboard table is shipped with the Console, but not assembled.
4.3 System Lifting and Rigging Restrictions
Lift-Gate and Rollback Truck Deliveries
Delivery to a facility without a loading dock can generally be serviced by a lift-gate or rollback
truck. A lift-gate delivery truck requires a lift gate rated for a 3-ton capacity.
If a rollback delivery truck is used, a GE representative shall personally supervise the delivery of
the PET/CT scanner to ensure the system is safely delivered without damage. To avoid
damaging the gantry, the representative shall direct the driver to attach strapping to the lowest
point (not the wheels) of each dolly. When the gantry is lowered from the back of the delivery
truck, it shall be lowered at the slowest reasonable rate without jerking the gantry. Otherwise,
serious damage to the gantry could occur.
4.4 Shipping and Receiving
4.4.1 Handling Restrictions
• Forklift Restrictions: Never lift the gantry using a forklift under the gantry frame.
• Shock Restrictions: The system cannot tolerate shock or vibration. System components
cannot be tipped, dropped, or hoisted. The PM shall communicate these restrictions to
everyone involved with handling the system components.
• Rolling on Surfaces: System components shall be rolled across smooth surfaces

(sidewalks, parking lots, etc.) only. If a smooth surface is not available, then floor protection
should be used to move the system.

• Shipping Crate/Packaging Integrity: Do not damage or puncture the shipping crate or

packaging.
Floor Protection
To protect the floor during delivery, floor protection shall be used along the entire delivery path
and throughout the scan suite, where necessary.
4.4.2 Dollies
• U.S. Installations – Shipments within the United States typically involve the use of dollies for
moving the gantry and table. After completing the installation, return all dollies and the
gantry shipping cage to GE using the shipping document found in Box #1.
• Zero Clearance Dollies (Mini) (For CT Gantrys only) – Deliveries involving small elevators
with a depth of at least 2692 mm (106 in.) require zero clearance dollies. Zero clearance
dollies allow movement of the gantry in tight areas; avoid using them for normal dock or van
deliveries. To order zero clearance dollies, go to: http://www.umi-dollyshop.com.
• Tilting Dollies (for Patient Table) – Deliveries involving small elevators with a depth of at
least 2438 mm (96 in.) require tilting dollies. If storing the patient table prior to installation,
do not order tilting dollies as there is a limited number of dollies available. If you are unable
to obtain tilting dollies, substitute riggers in place of the dollies to deliver the table. To order
tilting dollies for the patient table, go to: http://www.umi-dollyshop.com.
• Installations Outside U.S. – For shipments outside the United States, customers may
purchase dollies at: http://www.umi-dollyshop.com. DO NOT return dollies or the gantry
shipping cage to the U.S. Instead, forward dollies and cage to the local GE office or
warehouse.
4.4.3 Delivery Temperature and Humidity Tolerance
NOTICE
Failure to adhere to temperature requirements during delivery and storage will
likely result in equipment damage.
Avoid extreme temperatures during system transportation and delivery.

When transporting the system, all packing material shall remain intact. Prevent extended
exposure of the system (maximum two weeks) to temperatures or humidity outside of the
following specifications:
• Temperature: -40º to +50º C (-40º to +122º F), inclusive
• Humidity: 5% to 95%, inclusive
After delivery to the scan suite and before unpacking any system components, allow 12 hours
for the equipment to adjust to room temperature.
4.4.4 Unpacking System
Do not remove any protective wrapper or packaging from any system component until all
construction is complete and all construction dust is removed from the installation site.
Retain the packaging surrounding the scanner desktop and UPS.

Do not remove the Console or Q.Core/PARC4 (Q.Core Power) from their shipping skids until
after they have been delivered to the CT equipment room.
4.5 Storage
If storing a system prior to installation, the system shall be stored in its original packaging in a
temperature and humidity controlled environment protected from water and dust. It is advised
that storage of the system be no longer than six months. If storage is going to exceed six
months, contact your PM for long-term storage procedures.
Table 1-3: Humidity and Ambient Temperatures for Storage*
Ambient temperature shall be maintained within a range of: +4 to +27° C (+40 to +80° F)
Maximum rate of change in the temperature shall be no greater than: 3° C per hour (+37° F)
Relative humidity (non-condensing) shall be maintained within a range of: 30 to 60% RH
Maximum rate of change in the relative humidity shall be no greater than: 5% RH per hour
* Delivery van/truck storage shall meet these same requirements.
NOTICE
Storage exceeding six months is not advised.

Chapter 2 Equipment Requirements

1 System Components
1.1 Component Weight/Load, Dimensions, and Center of Gravity
Table 2-1: System Component Weight/Load
System Compo‐ Net Weight Maximum Maximum Load Pattern mm (in.) Normal Method of Mounting mm
nent kg (lb) Uplift Load N Compressive (in.) (GE-supplied1)
(lb) load N (lb)
CT Gantry 1810 (3990) 0 4588 (1031) CT effective load area is 700 x Hilti Kwik-Bolt II 12.7 mm (1/2
(64 slice) 2013 (27.6 x 79.25) with four in.) diameter x 254 mm (10 in.)
round pads, each 63.5 (2.5) in long per P/N 2106573-2 at four
contact with the floor. leveling pads into concrete
floor.
CT Gantry 1682 (3700) 0 4895 (1100) Rectangular base plate 700 x Hilti Kwik-Bolt II 12.7 mm (1/2
(16 slice) 1966 (28 x 77) with four round in.) diameter by 203 mm (8 in.)
pads, each 63.5 (2.5) in contact long per P/N 2106573 at four
with floor. Individual pad load‐ leveling pads into the concrete
ings are 910 lb., 960 lb., 1040 floor.
lb., and 1090 lb.
PET Gantry 1968 (4339) 0 6101 (1250) While in the imaging position, Hilti Kwik-Bolt II 12.7mm (1/2
the effective PET load area is in.) diameter by 8 in. (203mm)
398 x 645 (15.7 x 25.4) with 7 long per P/N 2106573 at seven
pads each 63.5 (2.5) as well as leveling pads into concrete
2 pads that do not get anchored floor.
(support only)
Patient Table 1049 (2308) 890 (200) 4926 (1107) Rectangular base 550 x 2134 Hilti Kwik-Bolt II 12.7mm (1/2
Includes (21.7 x 84.0) with 6 round pads, in.) diameter per 8 in. (203 mm)
227 (500) each 63.5 (2.5) in contact with long per P/N 2106573 at four
Patient the floor. leveling pads into concrete
floor.
Power Distribu‐ 370 (813) 0 1070 (240) Four Casters support area of Casters are for positioning and
tion Unit (PDU) 711 x 559 (28 x 22). service. See Note 2.
Q.Core 87 (192) 0
PARC4 (Q.Core 246 (540) 0 737 (166) Rectangular base with four cas‐ Casters are for positioning and
Power) tors. service. See Note 2.
Console w/o 72 (159) 318 (71)

monitors
Monitor - LCD 10 (22)

(each)
Console Work‐ 76 (167)

space Table (with
2 monitors)
Optional Components
Universal Power 281 (619) 0 689 (155) Rectangular base 305 x 813 Casters are for positioning. Set
Supply (UPS) (22 x 32) with four castors, on floor. Adjust the six leveling
each in contact with the floor. pads on the floor.
Notes:
1.) Use the GE-supplied mounting hardware only if anchoring the system to 127 mm (5 in.) concrete floors.
2.) Seismic angle brackets are included and shipped with the PDU and PARC4 (Q.Core Power).
Chapter 2 Equipment Requirements 39

Table 2-2: System Component Dimensions
System Component A B C
Width mm (in.) Depth mm (in.) Height mm (in.)
PET-CT Gantry (overall) without Trailer 2235 (88) 1473 (58) 1930 (76)
Table (at max elevation; 1" [25 mm] below Gantry ISO 660 (26) 3454 (136) 1067 (42)
center)
Power Distribution Unit (PDU) 711 (28) 559 (22) 1067 (42)
Q.Core 470 (19) 740 (29) 655 (26)
PARC4 (Q.Core Power) Reconstruction Cabinet 616 (24.3) 1257 (49.5) 1422 (56)
Operator Console 470 (19) 740 (29) 655 (26)
Console Workspace Table (adjustable height) 1350 (53) 741 (29) 683-912 (27-36)
UPS 305 (12) 813 (32) 1219 (48)
1.2 System Component Diagrams

Illustration 2-1: Gantry and Table Dimensions
All dimensions are in millimeters; bracketed dimensions are in inches.
1 CT scan plane centerline
2 PET primary scan plane centerline
3 With Head Extender
40 1 System Components
Illustration 2-2: Power Distribution Unit (PDU) Dimensions
A Rear View 1 I/O Connections Panel
B Top View 2 AC Power Input Box
3 Rear vent access
4 Front

Illustration 2-3: Q.Core and Operator Console Dimensions
A Side View 1 Air out
B Front View 2 Air in
C Top View 3 Wall
4 Clearance (minimum)
Illustration 2-4: PARC4 (Q.Core Power) Reconstruction Cabinet Dimensions
A Front View 1 Air in (front of cabinet)
B Side View 2 Air out (top of cabinet)

Illustration 2-5: Console Workspace Table Dimensions
1 76 kg (167 lb)
1.3 System Component Center-of-Gravity Diagrams

Refer to Illustration 2-6 through Illustration 2-15 for the individual system component center-of-
gravity dimensions for the PET/CT system.
Illustration 2-6: CT/PET Gantry Center-of-Gravity (Side View)
1 Center of gravity for CT Gantry
2 Center of gravity for PET Gantry
3 Minimum thickness
Illustration 2-7: CT Gantry Center-of-Gravity (Top View – Plan at Base)
1 Center of gravity weight (16 Slice) = 1682 kg (3700 lb); Y = 39.96”
Center of gravity weight (64 Slice) = 1810 kg (3990 lb); Y = 39.96”

Illustration 2-8: PET Gantry Center-of-Gravity (Top View – Plan at Base)
1 Center of gravity weight = 1968 kg (4339 lb); Y = 22.69”
Illustration 2-9: Patient Table Center-of-Gravity (Side View)
1 Center of gravity weight = 1049 kg (2308 lb); includes 227 kg (500 lb) patient
2 Minimum thickness
Illustration 2-10: Patient Table Center-of-Gravity (Top View – Plan at Base)
1 Center of gravity weight = 1049 kg (2308 lb); includes 227 kg (500 lb) patient. Y = 21.3”
Illustration 2-11: Power Distribution Unit Center-of-Gravity (NGPDU)
A Front View 1 Seismic mounting holes
B Side View 2 Minimum air flow clearance
C Top View 3 Seismic floor mounting holes; 15 mm (0.6 in.)

Illustration 2-12: Q.Core and Operator Console Center-of-Gravity
A Side View 1 Air out
B Front View 2 Air in
C Top View 3 Wall
Illustration 2-13: PARC4 (Q.Core Power) Reconstruction Cabinet Center-of-Gravity
A Front View 1 Center of gravity weight = 246 kg (540 lb)
B Side View
Illustration 2-14: Uninterruptible Power Supply (UPS) Center-of-Gravity
B Top View (plan at base) 2 Pre-manufactured mounting bracket (by GE)
3 Minimum thickness

Illustration 2-15: Storage Cabinet Center-of-Gravity
B Side View 2 Minimum thickness
3 L 3" x 3" x 1/4" x 14" bracket mounted to cabinet frame with 4 - #12 S.M. screws (each
side)
2 Room Layout
2.1 Scan Suite Configuration
A scan suite, which includes a control room and a scan room, requires a minimum room size to
safely support all PET/CT service activities. An example of a typical system configuration is
detailed in Illustration 2-16.
Illustration 2-16: Typical Scan Suite Layout Configuration
All dimensions are in millimeters (mm) and inches (in.).
1 Control Room 4 Service Cabinet
2 Scan Room 5 PDU
3 Q.Core or PARC4 (Q.Core 6 Service Clearance

Power)
The enclosure (Patient Touch) Leakage Envelope, as detailed in Illustration 2-17, defines a
zone in the Scan Room only, where the enclosure leakage must be tested. Areas that fall
outside of this envelope DO NOT need to be tested. The intent of this graphic is to provide the
PM with a view of potential electrical devices, plumbing fixtures, hospital gas outlets, and metal
surfaces that may fall within this scan room envelope, which may require additional grounding
prior to customer turnover. [Height of envelope from floor-to-ceiling: IEC-2 = 2286.0 mm (7.5
Ft.), IEC-3 = 1829.0 mm (6.0 Ft.). UL60601-1 (2.12.20 DV Addition) and GE Healthcare
requirement.]
NOTE: The enclosure leakage envelope has nothing to do with Regulatory Work Space
Clearance or Safe Egress requirements for Service Personnel (NFPA 70E).

Illustration 2-17: Leakage Envelope – Scan Room
1 = PDU, A = Patient Care Perimeter Envelope, B = Equipment Perimeter, C = Width and Height
Reference Dimension [C]
— Width Height
IEC Ed 2 1829.0 mm (6.0 Ft.) 2286.0 mm (7.5 Ft.)
IEC Ed 3 1829.0 mm (6.0 Ft.) 1829.0 mm (6.0 Ft.)
2.2 Minimum Scan Room Sizing

2.2.1 Scan Room Operational Space Requirement
For a minimum scan room layout, the customer should consider room workflow, patient care
accessibility, critical-care equipment space requirements, and applicable local building codes.
Refer to the dimensions detailed in Illustration 2-16 and Illustration 2-17.
52 2 Room Layout
2.2.2 Scan Room Equipment Accessibility

Minimum scan room layout provides limited equipment accessibility on the left side of the
gantry, particularly when loading patients or when positioning equipment between the gantry
and wall. Refer to the dimensions detailed in Illustration 2-16 and Illustration 2-17.
2.3 Minimum Control Room Sizing
2.3.1 Control Room Considerations and Requirements
The control room shall be suitably sized for the scanner desktop. Refer to the dimensions
detailed in Illustration 2-16 and Illustration 2-17. The control room should also provide a
comfortable working environment for the operator. Refer to Chapter 4, HVAC Requirements.
2.3.2 Autoinjector Control Placement
Provide a suitable work area for placement of the autoinjector control, within reach of the
scanner desktop. Autoinjector controls vary in size, depending on the manufacturer. Refer to the
manufacturer’s installation instructions.
2.4 Control Room Scanner Desktop Requirements
2.4.1 Scanner Desktop Configuration
The scanner desktop shall remain in the same configuration it was shipped. System
components shall not be disassembled, removed, or rearranged.
Once the system is installed, do not relocate any system or operator components to a different
counter, table, or location in the room.
2.4.2 Scanner Desktop Clearance
To ensure the exhaust fans located on the back of the scanner desktop vent without obstruction,
maintain 152 mm (6 in.) of clear, unobstructed space along the sides of the desktop.
2.4.3 Scanner Desktop Power
No other electrical devices may be connected to the scanner desktop components. All other
devices shall be connected to their own electrical outlet or power source.
2.4.4 Scanner Desktop Cables
Scanner desktop cables shall remain as shipped. Cables cannot be cut or lengthened to
relocate the desktop monitor to a remote table or counter.

3 Hospital Equipment and Service Space Requirements

3.1 Clearances
3.1.1 Operational Clearances
Review operational clearances to verify daily use items will properly fit (beds, carts, wheelchairs,
etc.).
3.1.2 Emergency Medical Equipment Clearances
Consider clearances for emergency medical equipment.
3.1.3 Replacement Parts and Service Equipment Space
Prior to the installation of the system, verify there will be adequate space in the scan room to
receive and install all replacement parts and provide room for all service equipment that will be
used during the installation.
3.1.4 Ceiling Height Requirements
The minimum ceiling height above the table and gantry shall measure at least 2286.0 mm (90.0
in.), or the minimum distance allowed by local laws and codes, whichever is greater, when
measured from the floor to the finished ceiling.
3.2 Workplace Requirements
3.2.1 U.S. Code Requirements
The required service space, as noted in Illustration 2-18 and Illustration 2-19, has several
conditions defined by the (U.S.) National Electrical Code (NEC). These conditions are defined
by the wall type and accessibility/exposure to: electrical power panels, electrical outlets, surface
mounted conduits, plumbing, hospital gases, or surface ground points directly opposite exposed
CT equipment.
Work space clearances apply to equipment operating at 600V or less, where examination,
adjustment, servicing, and maintenance is likely to occur with live parts exposed. System
servicing requires a space for one service engineer to accomplish all system component
replacement tasks without the need of special tools or equipment.
There shall be sufficient working space in the scan room to allow adequate egress during
service operations that require both front and rear cover removal. If the customer and PM have
any concern that the site will not provide adequate work space for egress under these
conditions, the necessary provisions should be made to accommodate this event.
The customer shall maintain the required regulatory clearance distances and not use these
areas for storage. This applies during normal system operation and during service inspection
and routine maintenance.
This work space is defined where the cover has been removed in an area where service is
performed, with power applied to the system. The conditions of this space are as follows:
Service Space: Also defined as Working Space by: IEC/NFPA 70e (Table 110.26) 2011 Edition.
GE Healthcare also requires the following minimum work space requirements for the safe
servicing of the product:
54 3 Hospital Equipment and Service Space Requirements

Working Space: Work space for equipment operating at 600 Volts, nominal, or less, to ground,
and likely to require examination, adjustment, servicing, or maintenance while energized. Refer
to the conditions in Table 2-3 and Table 2-4.
IEC/NFPA 70e (Table 110.26) 2011 Edition GE Healthcare requires the following minimum work
space requirements for the safe servicing of the product.
Terms Defined for “Work Space Conditions”
• Grounded Surface/Wall: Made of concrete, masonry, brick, ceramic tile, or a wall that
contains surface mounted electrical boxes, conduits, or ducting.
• Ungrounded Surface/Wall: Made of wood or other insulated construction material that will
not create a path to ground when touched.
• Obstructions: Surface mounted floor ducts or other trip hazards, walls, pilasters, support
columns, and equipment covers stored temporarily that would block direct access to an exit
from the room.
• Head Clearance: Head clearance represents the height dimension of the work space, as
measured from the floor directly in front of the equipment to the ceiling (or overhead
obstruction). It requires a minimum of 1981 mm (78.0 in.), or the height of the equipment,
whichever is greater.
• Powered On Service – Work Space Egress - 712.0 mm (28.0 in.): Any work space around
the perimeter of the system or subsystem, shall have at least one unobstructed route to a
direct exit of the room. The width of the exit route shall not be less than 712.0 mm (28.0 in.)
along the entire length of the route. This emergency egress route must be free of
obstructions and trip hazards, including equipment covers that may have been removed for
service.
• Small Room – (Not Recommended): A condition of installation where the gantry may be
placed a minimum of 356.0 mm (14.0 in.) from a wall where access to electrical power or the
wall is not required. (Limited to the side of the gantry, opposite the Tube-Change side of the
gantry.)

Table 2-3: Work Space Conditions
Dimension Condition Condition Separation Distance

Number mm (in.)
If the depth of the working space is directly facing an ungrounded sur‐ 914.0 (36.0)
1 face or wall without live voltage panels (600V or less) and without sur‐
face mounted ducts or conduits.
If the depth of the working space is directly facing a grounded surface 1067.0 (42.0)
Length/Depth 2
or wall.
If the depth of the working space is directly facing a surface or wall with 1219.0 (48.0)
3 live voltage panels (600V or less), grounded surface mounted ducts, or
conduits.
Minimum width of the working space in front of the electrical equipment, 762.0 (30.0)
unless the width of the equipment is larger.
If the equipment is wider than 762.0 mm (30.0 in) the width of the Size of Equipment
Width 4
equipment shall become the width of working space.
The working space shall permit at least a 90 degree opening of equip‐ —

ment doors.
Minimum Height of the working space shall be clear and extend from 2000.0 (78.0)
the grade (floor), unless the height of the equipment is higher.
Height 5
If the equipment is taller than 2000.0 mm (78.0 in.), the required height Height of Equipment
of the working space shall become the height of the equipment.
Table 2-4: Small Room Condition
Small Room Condition Separation Distance

mm (in.)
Minimum distance required on the side of the gantry, opposite the Tube-Change side of the gantry. 356.0 (14.0)

Illustration 2-18: Work Space Conditions
A Condition 1 2 Exposed live parts
B Condition 2 3 Scanner or subsystem
C Condition 3 4 Grounded parts, concrete, etc.
1 Effectively insulated 5 A1, other electrical equipment power panels

Illustration 2-19: Small Room Condition
1 Effectively insulated
2 Scanner or subsystem
A Small Room Condition. No live parts to service on this side.
3.2.2 Cover Removal Clearance

System servicing requires sufficient space to remove all covers from the system.
3.3 Cover Clearance Requirements
3.3.1 Gantry Front Cover – Removal Clearance
Front cover removal requires a minimum clearance space of 3010 mm (118.5 in.). The cover is
removed using a pair of dollies that allow the service engineer to remove the cover from the
gantry, tilt the cover 90° to roll it to the foot end of the table, and then tilt the cover an additional
90° so it is upsidedown, relative to its normal installation position. Minimum service clearances
are a regulatory requirement.
3.3.2 Gantry Front Cover – Service Clearance
Once the front cover of the gantry is removed, the service engineer shall have the ability to
reposition the cover to an area that satisfies the minimum regulatory service clearance. The
cover cannot be placed in an area where it will encroach on the minimum service area.
3.3.3 Gantry Rear Cover – Removal Clearance
Rear cover removal requires the use of tilting cover dollies with a minimum clearance width of
2388 mm (94 in.) and a depth of 584 mm (23 in.). Minimum service clearance space allows the
service engineer to move the cover either straight back or off to one side of the table. The rear
cover and dollies cannot extend into the service clearance space, even if the system is
positioned diagonally. Minimum service clearances are a regulatory requirement.
3.4 Gantry Space Requirements
Specifications for Boom Assembly clearance arc are defined in Illustration 2-20. The Boom
Assembly is used during Tube and Detector replacement.

Illustration 2-20: Boom Assembly Clearances
1 CT Gantry
2 Table
3 Clearance radius
3.5 PDU Placement Requirements

When positioning the PDU, consider regulatory compliance. Also, refer to the room layout
illustrations in Room Layouts.
3.6 Scanner Desktop Placement Requirements
3.6.1 Scanner Desktop Depth
The site shall maintain a working space at all times, with a minimum depth of 1219 mm (48 in.),
extending the full width of the scanner desktop for service activity.
3.6.2 Scanner Desktop Operating Space
The console is on wheels. As some service activities require access to the rear of the console,
be sure to maintain sufficient space for moving the console to allow rear service access.
3.7 Q.Core Placement Requirements
The Q.Core unit is on wheels and is serviced from the left side. Power connections are located
in the rear.

3.8 PARC4 (Q.Core Power) Reconstruction Cabinet Placement Requirements

The PARC4 (Q.Core Power) Reconstruction Cabinet is on wheels and can be pulled away from
the wall for service. Power connections are brought in through an access panel on the bottom of
the cabinet. Front clearance must be at least 152 mm (6 in.) for input air flow. Do not block
upwards exhaust air flow on the top-rear area of the cabinet.
3.9 Trailer Requirements
Trailer is serviced from the right and left sides with power on and the gantry in the home
position. Gantry-expanded power-on service is not recommended.
3.10 Storage Cabinet Requirements
A storage cabinet is provided by GE Healthcare to store all supplied service equipment. (See
Table 2-5 or Table 2-6 for equipment list.) This storage cabinet should be located in the scan
room suite area for easy service access.
Table 2-5: Discovery 610 and 710 (64 slice) Storage Cabinet and Equipment
Item Size Weight (total)
Storage Cabinet 46 x 91 x 107 cm (18" D x 36" W x 42" H) 45.3 kg (100 lb) (approximately)
QA Phantom (water filled) 23 x 15 cm (9" x 6") 4.5 kg (10 lb)
Phantom Holder 25 x 25 cm (10" x 10") 9.1 kg (20 lb)
FE Documents & CD/DVD 4.5 kg (10 lb)
Stool 48 x 48 cm (19” x 19”) 1 kg (2 lb)
Blue Tote 81 x 51 x 32 cm (30" x 20’ x 17") 2 kg (4 lb)
Install Support Kit (box) 30 x 30 x 38 cm (12" x 12" x 15") 9.1 kg (20 lb)
Tube Hoist Kit 77 x 8 cm and 38 x 15 cm (30" x 3" and 15" x 6") 13.6 kg (30 lb)
Balance Weight Kit (2 boxes) 33 kg (73 lb)
Spatial Resolution Phantom 18 x 15 x 8 cm (7" x 6" x 3")
Table 2-6: Optima 560, Discovery 610 and 710 (16 slice) Storage Cabinet and Equipment
Storage Cabinet 46 x 91 x 107 cm (18" D x 36" W x 42" H) 45.3 kg (100 lb) (approximately)
QA Phantom (water filled) 23 x 15 cm (9" x 6") 4.5 kg (10 lb)
Phantom Holder 25 x 25 cm (10" x 10") 3.6 kg (8 lb)
FE Documents & CD/DVD 4.5 kg (10 lb)
35 CM Poly (Circle) 35 x 8 cm (14" x 3") 6.8 kg (15 lb)
48 CM Poly (Circle) 48 x 8 cm (19" x 3") 11.3 kg (25 lb)
Stool 48 x 48 cm (19” x 19”) 1 kg (2 lb)
Blue Tote 81 x 51 x 32 cm (30" x 20’ x 17") 2 kg (4 lb)
Install Support Kit (box) 30 x 30 x 38 cm (12" x 12" x 15") 9.1 kg (20 lb)
Tube Hoist Kit 77 x 8 cm and 38 x 15 cm (30" x 3" and 15" x 6") 13.6 kg (30 lb)
Balance Weight Kit (2 boxes) 33 kg (73 lb)

Spatial Resolution Phantom 18 x 15 x 8 cm (7" x 6" x 3")
3.11 Verify Site Print

The customer shall ensure all equipment, storage cabinets, countertops, and sinks appear on
the site print, in their proper location.

4 Anchoring
4.1 Anchoring Requirements – Non-Seismic Installation
WARNING
POTENTIAL FOR PATIENT INJURY!
AN IMPROPERLY SECURED TABLE MAY TIP, DISLODGING THE PATIENT.
PATIENT SAFETY DURING SYSTEM OPERATION REQUIRES PROPER
ANCHORING OF SYSTEM COMPONENTS.
4.1.1 Gantry, Patient Table, and Trailer Anchoring – Non-Seismic
The Gantry, Patient Table, and Trailer shall be securely anchored to the floor (see Illustration
2-21). The scanner desktop, Power Distribution Unit, and system recon cabinet (Q.Core or
PARC4 (Q.Core Power)) do not require anchoring to the floor in a non-seismic installation. Use
the floor template (p/n 5322810) or its dimensions to locate the Gantry, Patient Table, and
Trailer support positions within the scan room, making sure that any anchors that pass through
the supports clear all structural beams and interferences in the floor.
It is the responsibility of the buyer/purchaser of the system to have a licensed structural
engineer work in conjunction with a qualified contractor to use either the GE-supplied floor
anchor hardware or provide an equivalent anchoring system to mount the gantry and patient
table to the floor.
The buyer/purchaser shall consult a licensed architect, licensed structural engineer, qualified
contractor, or the PM to resolve all anchoring issues.
62 4 Anchoring
Illustration 2-21: Floor Mounting Detail
All dimensions are in inches; bracketed dimensions are in millimeters.
1 Heat shield thickness 4 Table centerline
2 PET side of heat shield 5 CT scan plane centerline
3 Cable access area 6 PET primary scan plane centerline
4.1.2 GE-Supplied Anchors

The GE-supplied anchors for the Gantry, Patient Table, and Trailer shall only be used for
mounting components to a concrete floor, in a non-seismic application. Refer to Illustration 2-22
for anchoring requirements.

Illustration 2-22: GE-Supplied Floor Anchor Cross-Section
1 Anchor Assembly
2 63.5 mm (2.5 in) diameter leveling pad

9.7 mm (0.38 in) height for short 8 inch rod
44.5 mm (1.75 in) height for long 10 inch rod
3 Floor depth
4 Minimum anchor embedment
5 Drill depth
6 For short 8 inch rod
7 For long 10 inch rod
4.1.3 Anchor Placement

Each floor anchor shall be installed to clear any structural object hidden or buried in the floor.
(Hidden objects could be floor beams, rebar, and concrete wire mesh.)
4.1.4 Minimum Number of Anchors
Non-Seismic installations shall use a minimum of eight floor anchors to mount the Gantry, four
floor anchors to mount the Patient Table, and five anchors to mount the Trailer. Any anchors
showing more than 21 mm (~0.9 in.) of thread above the torqued nut shall require the
installation of a second anchor in the closest adjacent mounting location. The second anchor
shall meet the same requirements in Illustration 2-22.
4.2 Anchoring Requirements – Seismic Installation
For a seismic installation, the buyer shall refer to all applicable state/local laws and building
codes. Buyer shall consult with structural engineer, site contractor, or architect for seismic
installation requirements. The purchaser can also contact a GEHC Project Manager to obtain
additional seismic calculations and information.
64 4 Anchoring
Chapter 3 Special Construction Requirements

1 Radiation Protection
1.1 X-Ray Radiation Protection
1.1.1 Shielding Requirements
A qualified radiological health physicist shall verify the scan room radiation barrier is properly
designed and installed, taking into consideration:
• Scatter radiation levels within the scanning room (see Illustration 3-1 to Illustration 3-4).
• Equipment placement
• Weekly projected workloads (# patient/day technique (kvp*ma))
• Materials used for construction of walls, floors, ceiling, doors, and windows
• Access to surrounding scan room areas
• Equipment in surrounding scan room areas (such as film developer, film storage)
• For small and medium filter survey, the 20 cm water phantom should be placed on the
phantom headholder inserted into the end of the patient table.
The four scatter surveys depict measured radiation levels within the scanning room at the
indicated distances, while scanning a 16cm CTDI phantom for the Head Scan mode and 32cm
CTDI phantom for the Body Scan Mode. The mAs, kV and aperture scaling factors are provided
in Table 3-1 and they can be utilized to adjust the exposure levels to the typical usage at the
site.
For example: The exposure level for a 120kV, 800 mA, 1sec scan at 50" (127 cm) away from
the scan plane is: 10.4 μGy (from Illustration 3-4) × 0.71 (from Table 3-1) × 800/100 (from Table
3-1) = 59.1 μGy.
NOTE: Actual measurements can vary. Expected deviation equals ±15%, except for the 5mA
and 1.25mm techniques, where variation may be greater (up to a factor of 2), due to
the inherent deviation in small values. The maximum deviation anticipated for tube
output equals ±40%. Isocurves already include the deviation margins.
Table 3-1: Shielding Requirements Scaling
Changed Parameter Multiplication Factor Changed Parameter Multiplication Factor
mAs new mAs/100 1.25 mm aperture 0.20
80 kV 0.24 2.5 mm aperture 0.22
100 kV 0.45 5 mm aperture 0.27
120 kV 0.71 10 mm aperture 0.38
140 kV 1.00 20 mm aperture 0.59
40 mm aperture 1.00
Chapter 3 Special Construction Requirements 65

1.1.2 System X-ray Scatter Envelope

Illustration 3-1: Typical Scatter Survey (Small & Medium Filter) - 16 Slice Optima 560, D610,
D710
Scale units: centimeters (inches). ISO-contour level units: µGy/scan. Technique: 140 kV, 100 mA, 1 sec, 4x5.00 mm
A Head Phantom (top view) B Head Phantom (side view)
66 1 Radiation Protection
Illustration 3-2: Typical Scatter Survey (Large Filter) - 16 Slice Optima 560, D610, D710
Scale units: centimeters (inches). ISO-contour level units: µGy/scan. Technique: 140 kV, 100 mA, 1 sec, 4x5.00 mm
A Body Scatter (top view) B Body Scatter (side view)

Illustration 3-3: Typical Scatter Survey (Small & Medium Filter) - 64 Slice D610, D710
Scale units: centimeters (inches). ISO-contour level units: µGy/scan. Technique: 140 kV, 100 mA, 1 sec, 40 mm aperature
A Head Phantom (top view) B Head Phantom (side view)
Illustration 3-4: Typical Scatter Survey (Large Filter) - 64 Slice D610, D710
Scale units: centimeters (inches). ISO-contour level units: µGy/scan. Technique: 140 kV, 100 mA, 1 sec, 40 mm aperature
A Body Phantom (top view) B Body Phantom (side view)
1.2 Gamma Ray Protection

A number of radioactive substances, of various levels of stability are used by the PET unit of the
PET/CT system. This material is necessary in imaging procedures. Before the suite is

operational, unstable material may be on the premises. It is very important to recognize that
clear and significant hazards from ionizing radiation may exist at the site, as it is undergoing
preparation. Other equipment may be in place and operational at this time. This may include
such equipment as X-ray systems and CT scanners (other than the CT Gantry within the
PET/CT system). Calibration source may be on the site at some time during the preparation
process, as well as after the PET imager has been put into operation. A cyclotron may be
operational at the site. Definite steps should be taken to ensure the safety of workers, patients,
and visitors, during all phases of the construction, installation and operation of the facility.
NOTE: By the time the site is ready to have radioactive material brought in, the licensing
process must be complete. The site must be properly licensed before receiving
radioactive material.
1.2.1 Protection of Equipment
It is important that background radiation be kept to a minimum. The coincidence detection used
in a PET system allows a moderate amount of external singles events. The PET/CT system has
been found to have less than 1% deadtime if the external field is below 1 mR/hr from a single
source. Because area background can be more general than a single source, a lower limit is
appropriate. If the area dose rate is maintained to less than 0.2 mR/hr (due to 511 or lower
energy gamma rays) at the covers, detector deadtime should not exceed 1%.
Radioactive sources must be stored in approved shielded containers. It is recommended that
any radioactive source not specifically designed to be housed in the gantry’s lead storage
container be stored in a separate room (hot lab) adjacent to, and accessible from, the Scan
Room. This hot lab should be near the cyclotron (if used). Doses should be prepared in the
same area.
Consideration should be given to the placement of the gantry in relation to existing X-ray,
Magnetic Resonance, or Nuclear diagnostic equipment. Magnetic interference above 1.0 gauss,
at the surface of PET components, can adversely affect the image quality. Good shielding
techniques must be implemented in order to avoid this type of interference.
Some procedures involve the use of radioactive water. This will result in the patient exhaling
radioactive carbon dioxide. This carbon dioxide must be contained in order to avoid adversely
affecting the image quality. Some PET procedures require the use of radioactive gases. This too
can result in compromising image quality if not properly controlled.
1.2.2 Protection of Personnel
The escape of radioactive gases, if not properly confined, can cause unnecessary exposure to
clinical staff. All sources must be properly stored in appropriate enclosures to provide adequate
protection to all in the suite.
1.2.3 Barriers, Partitions and Shielding
Appropriate barriers such as walls, lead-shielded glass, lead shields etc. must be installed to
protect staff from unnecessary exposure to radiation. A qualified radiological health physicist
must be consulted in the design of walls and safety barriers to assure proper attenuation.
Keep in mind that patients become significant sources of radioactivity. Consideration should be
given to maximize the distance between the patient and operator during the uptake and
acquisition phases of scan procedures.
1.2.4 External Sources of Radiation

A number of common radio nuclides are used in the PET/CT system. These radio nuclides are
either produced at the site or brought to the site from an outside source. In either case, these
nuclides have relatively short half-life (2 min. to 110 min.) and as such decay to benign levels
fairly quickly. Typical positron emitting isotopes include: Carbon-11, Nitrogen-13, Oxygen-15,
and Fluorine-18.
1.2.5 Dose Rate from Radioactive Pin Source
The PET/CT system uses one radioactive pin source during calibration and the Daily QA Check.
During normal operation, the source pin remains in storage in a shielded container inside the
PET trailer. The system automatically withdraws the source from its container before each use,
and is automatically returned to the container after each use.
The dose rates described in this document are estimates, based on measurements taken under
specific measurement conditions, described in detail for each measurement. Since the
measurement conditions vary at every scanner installation (due to differing room geometries,
the presence of other equipment or shielding material, etc.), use these measurements as
guidelines only.
PET images are generated by measuring radiation resulting from electron positron annihilation
events within the patient. No external radiation source is required to generate this data. The pin
radiation source is never used during a patient scan.
The system uses the source pin to:
• Calibrate the scanner’s detectors and electronics.
• Assess the relative performance of the scanner’s detector channels, so differences in

individual detector efficiency can be accommodated during reconstruction.
The PET scanner uses a radioactive source pin that contains Ge68, an isotope with a half-life of
270.8 days. The radioactive source pin is referred to as “low activity pin.” The pin has an initial
activity level of 10MBq (0.27mCi) ± 20% for Optima 560 and Discovery 610, and 18.5MBq
(0.5mCi) ± 20% for Optima 560 FX, and Discovery 710.
Refer to Illustration 3-5. During normal system operation, the radioactive source pin resides in a
storage container, located inside the PET Trailer, at the rear of the PET/CT gantry.
Illustration 3-5: Source Pin Storage Location
1 PET Trailer (Source Pin stored inside)

When the pin is in use, it is located inside the gantry near the wall of the patient port. Depending
on the task the pin is performing, it may be held in a fixed location or rotated around the
circumference of the patient port at a speed of up to 20 revolutions per minute (one revolution
per three seconds). The pin is transferred from the storage container to its position near the
patient port, and returned to the storage container after use, by a mechanical system under
software control. Radiation indicators are displayed on both the gantry control panels and the
operator’s keypad when the pin source leaves the storage container.
1.2.5.1 Dose Rates with Pin Source Stored
When the radioactive source pin is stored in the lead container, and no other sources are
present in the scanner room, the maximum dose rates on the PET/CT system are directly over
the source loader. The PET/CT system uses one pin with an initial activity level of 10MBq
(0.27mCi) ± 20% or less for Optima 560 and Discovery 610, and 18.5MBq (0.5mCi) ± 20% for
Optima 560 FX, and Discovery 710. The exposure rate at the cover is specified to equal 2mR/hr
or less.
1.2.5.2 Dose Rates with Pin Source in Use
The dose rates were measured in the following conditions:
• Pin source rotating around the patient port.
• Patient table lowered to its lower limit (55 cm above the floor).
• All measurements were taken at a height equal the center of the patient port.
The results of these experiments, measured along the central axis of the scanner, are
summarized in Table 3-2. (Distances are measured from the front-most imaging slice; positive
distance is in the direction towards the scanner table.)
Table 3-2: Dose Rate at Specified Distances
Distances +3 m +2 m +1 m Front Slice -1 m -2 m
Dose rate per mCi mR/hr/mCi 0.07 0.14 0.75 5.46 0.68 0.68
Illustration 3-6: Distance Measurement Location
All dimensions are in meters; bracketed dimensions are in inches.
1.2.6 PET Alignment (VQC) Phantom

The PET Alignment (VQC) phantom is used during the Check Image Alignment procedure. This
special phantom contains spheres (commonly referred to as “marbles”). The five (5) small
spheres embedded in the phantom are a source of very low radiation (0.7 MBq Germanium-68
per sphere; total 3.5 MBq for p/n 5308767 phantom). The average life of the phantom is 2.5 to
4.0 years. Individuals using this phantom must be trained to handle radioactive materials as well
as maintain proper source handling procedures while handling the phantom. This may include
local site-specific procedures for the safe handling of radioactive material.

2 Electromagnetic Interference (EMI) Consideration

2.1 Electromagnetic Interference (EMI) System Placement
If you know of, or suspect, the presence of excessive electromagnetic interference (EMI),
consult your GE Healthcare PM or GE Sales and Service for recommendations to reduce EMI
fields. Consider the following to reduce EMI:
• EMI field strength decreases rapidly with distance from the source of the electromagnetic
field.
• EMI from a three-phase transformer is much less than a bank of three single-phase
transformers of equivalent power.
• Large electric motors are a substantial source of EMI.
• High-powered radio signals are a source of EMI.
• Maintain good shielding of cables and electronic cabinets.
• Consider and measure EMI where the facility power is running near the scan room.
• Pay attention to power substations and high-voltage power lines near the scan facility.
• If you have any concerns, measure for all EMI to confirm the site meets all required
specifications.
2.1.1 EMI – Gantry

The gantry shall be located in an area where the ambient static magnetic field is less than 10E-4
tesla (1000 milligauss) and the ambient AC magnetic field is less than 10E-6 tesla (10
milligauss); otherwise, EMI will affect the image quality of the scanner.
2.1.2 EMI – PDU
The gantry or patient table shall not be placed within 0.3 meters (12 in.) of the power distribution
unit.
Sensitive electronics shall not be placed within 1.0 m (39 in.) of the power distribution unit.
2.1.3 EMI – Scanner Desktop/Computer Equipment
The scanner desktop and its associated computer equipment shall be located in an area where
the ambient static magnetic field is less than than 10E-3 tesla (10,000 milligauss).
2.1.4 Electromagnetic Immunity
The system is intended for use in the electromagnetic environment specified in Table 3-3. The
customer, or the user of the system, shall ensure the system is used in such an environment.
74 2 Electromagnetic Interference (EMI) Consideration

Table 3-3: Electromagnetic Immunity
Immunity Test EC 60601–1–2 Test Compliance Level Electromagnetic Environment Guidance

Level
Electrostatic discharge ± 6 kV contact ± 6 kV contact Floors shall be concrete. If floors are covered with synthet‐
(ESD) IEC 61000-4-2 ± 8 kV air ± 8 kV air ic material, the relative humidity should be at least 30%.
Electrical fast transient/ ± 2 kV for power ± 2 kV for power sup‐ Mains power quality should be a typical commercial or
burst IEC 61000-4-4 supply lines ply lines hospital environment.
± 1 kV for input/ out‐ ± 1 kV for input/ out‐
put lines put lines
Surge IEC 61000-4-5 5 ± 1 kV differential ± 1 kV differential Mains power quality should be a typical commercial or
mode mode hospital environment.
± 2 kV common ± 2 kV common
mode mode
Voltage dips, short inter‐ < 5 % UT (> 95% dip < 5 % UT (> 95% dip Mains power quality should be a typical commercial or
ruptions and voltage var‐ in UT) for 5 sec in UT) for 5 sec hospital environment. If the user of the system requires
iations on power supply continued operation during power mains interruptions, it is
input lines IEC 61000-4- recommended that the system is powered from an uninter‐
11 ruptible power supply or a battery.
Power frequency (50/60 3 A/m 3 A/m Power frequency magnetic fields should be at levels char‐
Hz) magnetic field IEC acteristic of a typical location in a typical commercial or
61000-4-8 hospital environment.
Conducted RF IEC 3 VRMS 150 kHz to 3 V 150 kHz to 80 Do not use portable and mobile RF communications
61000-4-6 80 MHz MHz equipment closer to any part of the system, including ca‐
Radiated RF IEC 3 V/m 150 kHz to 80 3 V/m 150 kHz to 80 bles, than the recommended separation distance calculat‐
61000-4-3 (Alternative MHz MHz ed from the equation appropriate for the frequency of the
method: Full range IEC transmitter.
61000-4-21 test in lieu of Recommended Separation Distance:
Large, Permanently- In‐ See Table 3-4 where P is the maximum output power rat‐
stalled Equipment ex‐ ing of the transmitter in watts (W), according to the trans‐
emption) mitter manufacturer and d is the recommended separation
distance in meters (m). Field strengths from fixed RF
transmitters, as determined by an electromagnetic site sur‐
vey,a should be less than the compliance level in each fre‐
quency range.b Interference may occur in the vicinity of
equipment marked with the following symbol:
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, ama‐
teur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electro‐
magnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field
strength in the location in which the system is used exceeds the applicable RF compliance level above, the system should be ob‐
served to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorient‐
ing or relocating the system.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
2.1.5 Electromagnetic Separation Distance

Maintain the electromagnetic separation distance as described in Table 3-4 (between 150K to
2.5G Hz).

Table 3-4: Recommended Separation Distances
Rated Maximum Output Power Separation Distance (Meters) by Frequency of Transmitter

(P) of Transmitter Watts (W)
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
0.01 0.12 0.12 0.23
0.1 0.37 0.37 0.74
1 1.17 1.17 2.33
10 3.69 3.69 7.38
100 11.7 11.7 23.3
For transmitters rated at a maximum output power not listed above, the separation distance can
be estimated using the equation in the corresponding column, where power (P) is the maximum
output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE: At 80 MHz to 800 MHz, the separation distance for the higher frequency range
applies.
NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects, and people.
As an example, keep a 1 W mobile phone (800 MHz to 2.5 GHz carrier frequency) at
least 2.3 m from the PET/CT system (to avoid image interference risks).
Limitations Management:
Adhering to the distance separation recommended in (150 KHz to 2.5 GHz) reduces
disturbances recorded at the image level, but may not eliminate all disturbances. However,
when installed and operated as specified, the system maintains its essential performance by
continuing to acquire, display, and store diagnostic quality images safely.
2.1.6 Cable Shielding and Grounding
All interconnect cables to peripheral devices must be shielded and properly grounded, except
when technologically prohibited. Use of cables not properly shielded and grounded may result in
the equipment causing radio frequency interference.
GE Healthcare is not responsible for any interference caused by using other than recommended
interconnect cables or panels, or by unauthorized changes or modifications to this equipment.
Unauthorized changes or modifications could void the users' authority to operate the equipment.
2.2 Electromagnetic Emission
This equipment complies with IEC 60601-1-2 Edition 3 (2007) EMC standard for medical
devices.
NOTE: This system complies with the EMC standard when used with supplied cables. If
cables of different lengths are required, contact your PM. Cables cannot be cut,
shortened, lengthened, or spliced.
The system is suitable to be used in an electromagnetic environment, in compliance with the
limits and recommendations provided in Table 3-5.
76 2 Electromagnetic Interference (EMI) Consideration

Table 3-5: Electromagnetic Compliance
Emissions Test Compliance Electromagnetic Environment Guidance
RF emissions CISPR 11 Group 1 The system uses RF energy only for its internal function. Therefore, its RF
emissions are very low and not likely to cause interference in nearby electronic
equipment.
RF emissions CISPR 11 Class A When installed in such a shielded location, the scanner is suitable for use in all
establishments other than domestic, and those directly connected to the public
low-voltage power supply network that supplies buildings used for domestic
purposes.
Harmonic emissions IEC N/A N/A

61000-3-2
Voltage fluctuation/ flicker emis‐ N/A N/A

sions IEC 61000-3-2

3 Vibration Isolation
3.1 Scanning Facility Vibration Isolation
The scanning facility shall be isolated from vibration such as; hospital power plants, pumps,
motors, air handling equipment, air conditioning units, nearby rooms with exercise equipment or
where exercise occurs, hallway foot traffic, elevators, parking lots, roads, subways, trains, and
heliports; otherwise, vibration will affect the image quality of the scanner.
3.2 Frequency/Vibration Range
CT systems are sensitive to vibration and may display limited performance if exceeding the
vibration limits listed below. The band of frequencies in which systems exhibit the most
sensitivity appears at or near the resonant frequencies of the gantry and the patient table, the
latter of which varies depending on patient mass and location. These frequencies fall within the
following ranges:
• Patient Table: 2 – 10 Hz
• Gantry: 8 – 14 Hz
Floor vibration from any source shall not exceed the levels detailed in Illustration 3-7 and
Illustration 3-8, as represented by the solid line labeled CT Scanner/Table. These illustrations
compare this limit to the limits of what the AISC (American Institute of Steel Construction) and
the ISO (International Organization for Standardization) call Class A (VC-A) and Class B (VC-
B).
78 3 Vibration Isolation
Illustration 3-7: Allowable floor vibration in acceleration units compared to ISO class A and B
limits
A Acceleration [mm/s², rms] Frequency [Hz] Acceleration [mm/s2, rms]
B One-Third-Octave Band Center Frequency [Hz] 42 2.5
1 VC-A (50 µm/s) 10 2.5
2 CT Scanner/Table 12.5 3.1
3 VC-B (25 µm/s) 16 5
80 25

Illustration 3-8: Allowable floor vibration in velocity units compared to ISO class A and B limits
A Velocity [µm/s, rms] Frequency [Hz] Velocity [um/s, rms]
B One-Third-Octave Band Center Frequency [Hz] 4 100
1 VC-A (50 µm/s) 10 40
2 CT Scanner/Table 12.5 40
3 VC-B (25 µm/s) 16 50
80 50
80 3 Vibration Isolation
4 Other Construction Considerations

4.1 Patient Viewing Window Dimensions
The recommended patient viewing window is: 1219 mm wide x 1067 mm high (48 in. x 42 in.).
4.2 Support Structure Installation
Approved steelwork or equivalent support structure for mounting equipment to walls, ceilings,
and floors shall be installed prior to the system installation.
4.3 Chemical Contamination Concerns
WARNING
THE SILVER, COPPER, GOLD FILMS USED IN THE CT SYSTEM ARE
ESPECIALLY SENSITIVE TO CHEMICAL CONTAMINATION.
THE PRESENCE OF SULFIDE, CHLORIDE AND NITRATE CONTAMINATES
(WITH SULFUR BEING THE MOST DAMAGING), CAN DAMAGE THE CT
SYSTEM.
IF HIGH LEVELS OF CONTAMINATES EXIST, CONSIDER INSTALLING AN
APPROPRIATE AIR FILTRATION SYSTEM.
The scanner shall not be installed in the same room with a wet film processor. Certain scanner
components could become contaminated by the chemicals contained in the processor.
Ensure any sulfide, chloride, or nitrate contaminate levels are at acceptable levels (Class 1).
See IEC 60654-4 for air quality guidelines.
4.4 Finished Wall Requirement
4.4.1 Wall Paint
The scan and control room walls shall be painted prior to the system installation.
4.4.2 Wall Paint - Exception
A primer coat of paint is acceptable for system installation. After the system is installed, any final
coats of paint shall be applied by brush. Spray painting in not permitted as it can seriously
damage CT system components.
NOTE: Spray painting in not permitted. Spray painting can seriously damage CT system
components.
4.5 Option Requirements
4.5.1 Non-GE Installed Options
Buyer/purchaser shall confirm all non-GE installed options have been reviewed and final
locations determined. Prior to system installation, the buyer/purchaser shall be responsible for
pre-installing all ceiling mounting plates/pedestals for non-GE installed options prior to system
delivery.
4.5.2 GE Options
Buyer/purchaser shall confirm all GE-installed options have been reviewed and final locations
determined.

4.5.3 Options Power and Control Cables

Buyer/purchaser shall install all power source/connections and all control cables for all options
prior to system delivery.
82 4 Other Construction Considerations

Chapter 4 Environmental Requirements (HVAC)

1 HVAC Requirements
The following standard is referenced in this section: IEC 60654-4
1.1 Climate Requirements
1.1.1 Air Quality
All construction, finish, and construction cleanup work of the scanner suite shall be completed
prior to the installation of the CT system to prevent exposing the system to construction material
contamination.
1.1.1.1 Construction Dust Concerns
Ensure NO construction dust occurs in or immediately around the scan suite. Avoid:
• concrete dust
• drywall dust
• ceiling tile dust
• sawdust or wood shavings
• dust tracked into CT suite from adjoining rooms
Failure to protect the CT system from these types of dust may result in damage to the system
and early system failure.
1.1.1.2 Chemical Contamination Concerns
WARNING
THE SILVER, COPPER, GOLD FILMS USED IN THE CT SYSTEM ARE
ESPECIALLY SENSITIVE TO CHEMICAL CONTAMINATION.
THE PRESENCE OF SULFIDE, CHLORIDE AND NITRATE CONTAMINATES
(WITH SULFUR BEING THE MOST DAMAGING), CAN DAMAGE THE CT
SYSTEM.
IF HIGH LEVELS OF CONTAMINATES EXIST, CONSIDER INSTALLING AN
APPROPRIATE AIR FILTRATION SYSTEM.
The scanner shall not be installed in the same room with a wet film processor. Certain scanner
components could become contaminated by the chemicals contained in the processor.
It is the responsibility of the buyer/purchaser to insure any sulfide, chloride, or nitrate
contaminate levels are at acceptable, low levels (Class 1). See IEC 60654-4 for air quality
guidelines.
1.1.2 Temperature and Humidity Requirements
Ensure the site provides an HVAC system capable of maintaining the temperature and humidity
requirements as specified in Table 4-1 and Table 4-2. The environmental conditions at the site
shall be maintained at all times (including overnight, weekends, and holidays). Environmental
Chapter 4 Environmental Requirements (HVAC) 83

conditions apply to the Table, Gantry, Power Distribution Unit, Q.Core/PARC4 (Q.Core Power)
and scanner desktop.
NOTE: Exceeding the environmental specifications may adversely affect system operation
and image quality.
Table 4-1: System Temperature Limits
Maximum allowable ambient room temperature: 26ºC (79ºF)
Recommended ambient room temperature: 22ºC (72ºF)
Minimum allowable ambient room temperature: 18ºC (64ºF)
NOTE: Be certain to account for ANY cooling equipment cycle-control range, ensuring that
the maximum and minimum ambient room temperatures do not exceed those shown
in Table 4-1 during room thermal cycling. For example, if the HVAC is capable of ± 2º
C control, then the limits would be 20º C - 24º C to maintain absolute limits.
Table 4-2: Humidity (Scan and Control Rooms)
Maximum allowable non-condensing relative humidity: 60%
Minimum allowable non-condensing relative humidity: 30%
1.1.3 Altitude Operating Range

The system shall be operated within an altitude range of -150 m to 2400 m (-492 ft. to 7875 ft.)
sea level.
1.1.4 Environmental Conditions Verification
The temperature and humidity of the installation site shall be recorded before and after system
installation to verify the environmental conditions of the site are met. Any necessary changes
shall be made to maintain the proper environmental conditions.
1.1.5 Patient Comfort
Consider patient comfort needs when designing or modifying the HVAC system for the scan
suite. To prevent cold air from venting onto patients, position air supply ducts in exam room so
they do not discharge onto the patient Table. Position ducts over Gantry.
1.2 Heat Output
Table 4-3 details the heat load produced by the PET/CT system and its various components.
Use the BTU/Wattage ratings listed to determine the requirements of the HVAC system.
• Gantry air INTAKE occurs along the BOTTOM of the Gantry.
• Gantry air EXHAUST occurs along the TOP of the Gantry.
• PARC4 (Q.Core Power) air INTAKE occurs along the FRONT of the PARC4 (Q.Core
Power). PARC4 (Q.Core Power) air EXHAUST occurs at the TOP of the PARC4 (Q.Core
Power).
Table 4-3: System Heat Load*
System Components Maximum BTU/HR Maximum Kilowatts
84 1 HVAC Requirements
Scan Room:
CT Gantry 18766 5.50 kW
PET Gantry 5971 1.75 kW
Table 1024 0.30 kW
Power Distribution Unit (PDU) 3400 1.00 kW
Q.Core (Recon Cabinet) 2457 0.72 kW
PARC4 (Q.Core Power) (Reconstruction Cabinet) 6824 2.0 kW
Scan Room Subtotal: 31618 9.27 kW

(35985 with PARC4 (Q.Core (10.55 with PARC4 (Q.Core
Power)) Power))
Control Room:
Operator Console 2860 0.84 kW
LCD Monitor (2 units, 170 BTU/50 Watts each) 340 0.10 kW
Peripheral Media Tower (PMT) 425 0.13 kW
Control Room Subtotal: 3625 1.07 kW
System Total 35243 10.34 kW

(39610 with PARC4 (Q.Core (11.62 with PARC4 (Q.Core
Power)) Power))
* Does not include heat load from room lighting, non-PET/CT equipment, personnel, etc.
1.3 Air-Handling System Initial Start-Up Considerations
Prior to the initial start-up of the scan suite air-handling system, ensure the air-handling system
ducts and filters are thoroughly clean of dust and other potential airborne contaminants.
After new construction or scan suite renovation, the air-handling ventilation system, on initial
startup, could blow dust and other airborne contaminates throughout the scan suite, potentially
damaging the PET/CT scanner.
Chapter 4 Environmental Requirements (HVAC) 85

86 1 HVAC Requirements
Chapter 5 Electrical Requirements

1 Power Requirements
1.1 Regulations
NFPA 70E Standard
All electrical work shall comply with NFPA 70E: Standard for Electrical Safety in the Workplace.
1.2 Disconnects
1.2.1 Emergency Off Switch
The A1 mains disconnect shall provide over-current protection for the entire system and have at
least one Emergency OFF switch within the scan suite, near the scanner desktop.
1.2.2 Local Disconnects
The A1 mains disconnect with Lock-out and Tag-out (LOTO) capability shall be installed within
the scan suite. See Illustration 5-1.
Illustration 5-1: Typical Primary Power Disconnect (A1) – Fusible Disconnect and Magnetic
Contactor
Chapter 5 Electrical Requirements 87

1.3 Electrical and Junction Boxes

All electrical boxes and junction boxes shall be installed as specified by the architectural,
mechanical, or electrical drawings associated with the design of the site.
1.4 Power Feed and Overcurrent Requirements
1.4.1 Power Feed
The system shall operate on a three-phase electrical power supply input that is provided with a
4-wire grounded-wye configuration. No delta configuration is available. Qualified personnel shall
verify the power transformer and feeder lines (at the point of take-off) leading to the PET/CT
scanner, meet all requirements stated in this document.
1.4.2 Voltage
(For 64 Slice Discovery 610, Discovery 710) Voltage range: 380 to 480 VAC
(For 16 Slice Optima 560, Discovery 610, Discovery 710) Voltage range: 200/220/240 VAC;
380-480 VAC
1.4.3 Frequency
Frequency ranges: 50 or 60 Hz, +/- 3 Hz
1.4.4 Average Power Demand at Maximum Duty Cycle
(For 64 Slice Discovery 610, Discovery 710) Average power demand at maximum duty cycle:
15.5 kVA
(For 16 Slice Optima 560, Discovery 610, Discovery 710) Average power demand at maximum
duty cycle: 10 kVA
1.4.5 Maximum Power Demand
(For 64 Slice Discovery 610, Discovery 710) Maximum power demand is 150 kVA at 0.85 PF at
a selected technique of 140 kV and 715 mA.
(For 16 Slice Optima 560, Discovery 610, Discovery 710) Maximum power demand is 90 kVA at
0.85 PF at a selected technique of 140 kV and 380 mA.
1.4.6 Under voltage Release Control
The preferred disconnect, will utilize under voltage release control, rather than shunt trip
devices.
1.4.7 Overcurrent Protection
To prevent power loss to other loads during an unexpected system fault, the power feeder shall
have overcurrent protection such that the downstream overcurrent protection devices clear the
fault before an up-stream overcurrent protection device opens.
1.4.8 Voltage Regulation Effects
To minimize voltage regulation effects, keep power wiring between the facility main distribution
panel and the PDU as short as possible.
88 1 Power Requirements
1.4.9 Load Regulation

Total load regulation, measured at the PDU input terminals, shall not exceed 6%.
1.5 Phase Imbalance
The difference between the highest line-to-line voltage and lowest line-to-line voltage shall not
exceed 2% of the lowest line-to-line voltage.
1.6 Sags, Surges, and Transients
1.6.1 Sags and Surges
(For 64 Slice Discovery 610, Discovery 710) Sags and surges of the power line shall not exceed
the absolute range limits show in Table 5-1.
(For 16 Slice Optima 560, Discovery 610, Discovery 710) Sags and surges of the power line
shall not exceed the absolute range limits show in Table 5-4.
1.6.2 Transient Voltage
The maximum transient voltage is 1500 V peak.
1.7 Power Source Configuration
1.7.1 Neutral Wire
If a neutral wire is used, it shall be terminated in the A1 disconnect.
1.7.2 Dedicated Feeder
A dedicated main distribution panel (A1 Mains) shall be used to supply power to the scanner.
The A1 mains shall be located in the same room as the PDU.
1.7.3 Protective Disconnect Device Location
The protective disconnect shall be located within 10 m (32 ft.) of the PDU and be visible to
personnel servicing the PDU.
1.7.4 Protective Disconnect Device with LOCK-OUT/TAG-OUT
The National Electrical Code (NFPA 70) states there shall be a protective disconnect device
with a LOCK-OUT and TAG-OUT provision in the power supply line leading to the PDU.
1.8 Dedicated Distribution Transformer
1.8.1 Dedicated Feeder
It is recommended a dedicated distribution transformer from the facility's main isolation
transformer supply power to the PET/CT Scanner.
1.8.2 Power Distribution Transformer
(For 64 Slice Discovery 610, Discovery 710) The minimum recommended size for a dedicated
distribution transformer is: 225 kVA, rated 2.4% regulation at unity power factor. Resultant
maximum allowable feeder regulation is 3.4%.

(For 16 Slice Optima 560, Discovery 610, Discovery 710) The minimum recommended size for
a dedicated distribution transformer is: 112.5 kVA, rated 2.4% regulation at unity power factor.
Resultant maximum allowable feeder regulation is 3.4%.
1.8.3 Using an Existing Distribution Transformer
Do not use an existing distribution transformer to power a system if other X-ray equipment,
using rapid film changers, is connected to the existing transformer.
1.9 System Power Requirements (64 Slice Discovery 610, Discovery 710)
The customer shall ensure the site meets all minimum system power requirements listed below
before installation can begin.
• Maximum power demand = 150kVA @ 0.85 PF: at a Selected Technique of 140 kV, 715
mA.
• Continuous (average) power demand at maximum duty cycle = 15.5 kVA.
• Maximum allowable total source regulation is 10%.

Table 5-1: Nominal Line Voltage Ranges (64 Slice Discovery 610, Discovery 710)
Nominal line voltage MUST fall within ONE of these ranges.
Nominal Line Voltage 380 400 420 440 460 480
Hi-Line Limit, +10% 418 440 462 484 506 528
Lo-Line Limit, -10% 342 360 378 396 414 432
Continuous Line Current 38 36 34 33 31 30
Momentary Line Current 228 217 206 197 188 180
Maximum Line Current 253 241 229 219 209 200
Minimum Recommended Circuit Protection Rating 150 150 150 125 125 125
Table 5-2: Minimum Feeder Wire Size (64 Slice Discovery 610, Discovery 710)
Feeder Length (Power Substation Minimum Feeder Wire Size, AWG or MCM (sq. mm)/ VAC
to A1 Disconnect)
380 VAC 400 VAC 420 VAC 440 VAC 460 VAC 480 VAC
15 m (50 ft) 1/0 (55) 1/0 (55) 1/0 (55) 1 (45) 1 (45) 1 (45)
30 m (100 ft) 1/0 (55) 1/0 (55) 1/0 (55) 1 (45) 1 (45) 1 (45)
46 m (150 ft) 1/0 (55) 1/0 (55) 1/0 (55) 1 (45) 1 (45) 1 (45)
61 m (200 ft) 1/0 (55) 1/0 (55) 1/0 (55) 1 (45) 1 (45) 1 (45)
76 m (250 ft) 2/0 (70) 2/0 (70) 1/0 (55) 1/0 (55) 1 (45) 1 (45)
91 m (300 ft) 3/0 (85) 3/0 (85) 2/0 (70) 2/0 (70) 1/0 (55) 1/0 (55)
107 m (350 ft) 4/0 (100) 3/0 (85) 3/0 (85) 2/0 (70) 2/0 (70) 1/0 (55)
122 m (400 ft) 250 (125) 4/0 (100) 3/0 (85) 3/0 (85) 3/0 (85) 2/0 (70)
NOTE: In all cases the recommended ground wire is a 1/0 (55 sq. mm) ground wire.
Table 5-3: Minimum Sub-Feeder Wire Size (64 Slice Discovery 610, Discovery 710)
Sub-feeder Length (A1 to PDU) Minimum Sub-feeder Wire, AWG or MCM (sq. mm)
380 VAC 400 VAC 420 VAC 440 VAC 460 VAC 480 VAC
9.75 m (32 ft) 1/0 (55) 1/0 (55) 1/0 (55) 1 (45) 1 (45) 1 (45)
The information in Table 5-1, Table 5-2, and Table 5-3 (above) assumes the use of copper
wire, rated 75° C and run in steel conduit. All ampacity is determined in accordance with the
National Electrical Code (NFPA 70), Table 310-16 (2002). The ampacity of the circuit
protection device listed above determines the minimum feeder size, except where total
source regulation limits require a larger size.
NOTE: Power feeders running under the scan room floor, as well as power vault
substations under the floor, above the scan suite, or in adjacent rooms, may
cause excessive EMI fields. The responsibility for meeting all site EMI
requirements rests with the customer.
1.10 System Power Requirements (16 Slice Optima 560, Discovery 610, Discovery
710)
The customer shall ensure the site meets all minimum system power requirements listed below
before installation can begin.
• Maximum power demand = 90kVA @ 0.85 PF: at a Selected Technique of 140 kV, 380 mA.
• Continuous (average) power demand at maximum duty cycle = 10 kVA.
• Maximum allowable total source regulation is 6%.
Table 5-4: Nominal Line Voltage Ranges (16 Slice Optima 560, Discovery 610, Discovery 710)
Nominal line voltage MUST fall within ONE of these ranges.
Nominal Line Voltage 200 220 240 380 400 420 440 460 480
Hi-Line Limit, +10% 220 242 264 418 440 462 484 506 528
Lo-Line Limit, -10% 180 198 216 342 360 378 396 414 434
Continuous Line Current 58 52 48 30 29 27 26 25 24
Momentary Line Current 260 236 217 137 130 124 118 113 108
Maximum Line Current 289 262 241 152 144 137 131 126 120
Minimum Recommended Circuit Protection 150 150 150 110 110 100 100 90 90
Rating
Table 5-5: Minimum Feeder Wire Size (16 Slice Optima 560, Discovery 610, Discovery 710)
Feeder Length (Power Minimum Feeder Wire Size, AWG or MCM (sq. mm)/ VAC
Substation to A1 Dis‐
connect) 200 VAC 220 VAC 240 VAC 380 VAC 400 VAC 420 VAC 440 VAC 460 VAC 480
VAC
15 m (50 ft) 1/0 (55) 1/0 (55) 1/0 (55) 2 (35) 2 (35) 3 (30) 3 (30) 3 (30) 3 (30)
30 m (100 ft) 2/0 (70) 1/0 (55) 1/0 (55) 2 (35) 2 (35) 3 (30) 3 (30) 3 (30) 3 (30)
46 m (150 ft) 4/0 (100) 3/0 (85) 2/0 (70) 2 (35) 2 (35) 3 (30) 3 (30) 3 (30) 3 (30)

Feeder Length (Power Minimum Feeder Wire Size, AWG or MCM (sq. mm)/ VAC
Substation to A1 Dis‐
connect) 200 VAC 220 VAC 240 VAC 380 VAC 400 VAC 420 VAC 440 VAC 460 VAC 480
VAC
61 m (200 ft) 5/0 (125) 4/0 (100) 4/0 (100) 2 (35) 2 (35) 3 (30) 3 (30) 3 (30) 3 (30)
76 m (250 ft) 6/0 (170) 5/0 (125) 5/0 (125) 1 (45) 1 (45) 2 (35) 2 (35) 2 (35) 3 (30)
91 m (300 ft) 7/0 (215) 6/0 (170) 5/0 (125) 1/0 (55) 1/0 (55) 1 (45) 1 (45) 2 (35) 2 (35)
107 m (350 ft) 8/0 (275) 7/0 (215) 6/0 (170) 2/0 (70) 1/0 (55) 1/0 (55) 1 (45) 1 (45) 1 (45)
122 m (400 ft) 8/0 (275) 7/0 (215) 7/0 (215) 2/0 (70) 2/0 (70) 1/0 (55) 1/0 (55) 1/0 (55) 1 (45)
NOTE: In all cases the recommended ground wire is a 1/0 (55 sq. mm) ground wire.
Table 5-6: Minimum Sub-Feeder Wire Size (16 Slice Optima 560, Discovery 610, Discovery
710)
Sub-feeder Length Minimum Sub-feeder Wire, AWG or MCM (sq. mm)

(A1 to PDU)
200 VAC 220 VAC 240 VAC 380 VAC 400 VAC 420 VAC 440 VAC 460 VAC 480 VAC
9.75 m (32 ft) 1/0 (55) 1/0 (55) 1/0 (55) 2 (35) 2 (35) 3 (30) 3 (30) 3 (30) 3 (30)
The information in Table 5-4, Table 5-5, and Table 5-6 (above) assumes the use of copper wire,
rated 75° C and run in steel conduit. All ampacity is determined in accordance with the National
Electrical Code (NFPA 70), Table 310-16 (2002). The ampacity of the circuit protection device
listed above determines the minimum feeder size, except where total source regulation limits
require a larger size.
NOTE: Power feeders running under the scan room floor, as well as power vault substations
under the floor, above the scan suite, or in adjacent rooms, may cause excessive EMI
fields. The responsibility for meeting all site EMI requirements rests with the customer.
2 Grounding
The design of the scanner uses an equal potential grounding system. Illustration 5-2 and Table
5-7 detail the required ground system. Three primary grounding points exist, they include:
• A system power ground point located in the PDU.
• A reference ground point located between the gantry and the table base.
• A patient ground point located at the front of the table base.
The electrical contractor shall ground ALL patient-accessible metal surfaces to the same
potential as the A1 Disconnect. The electrical contractor shall bond the ground wire to any
intermediate distribution panel the ground wire passes through, in accordance with all local
codes.
Illustration 5-2: System Ground Map
Note: Shield/signal grounds are not shown.
A A1 Power Disconnect 1 To power vault ground
B Power Distribution Unit (PM) 2 Table/Gantry junction raceway
C Table (CT1) 3 Part of Gantry
D Q.Core or PARC4 (Q.Core Power) Re‐ 4 Rotating Assembly frame

construction Cabinet (PRC4)
E Gantry (CT2) 5 Tilt Mech
F Operator's Console/Computer (OC1) 6 Frame
7 Ground wire in supplied cable

Table 5-7: System Ground Points
Ground Points Description
Bonding Power from A1 to PDU The metal conduit, raceway, or armored cabling used to run power from the A1
Disconnect to the PDU shall be bonded in accordance to the NEC.
Dedicated Ground A dedicated 1/0 (55 mm2), or larger, insulated copper ground wire shall be instal‐
led between the main distribution panel and the PDU, in accordance with the
NEC.
Grounding Power, A1, and PDU All three-phase wires with ground running between the power source, the A1
Disconnect, and the PDU shall be installed in accordance to the NEC.
Maximum Resistance Between PDU and Facility The resistance between the PDU ground and the facility Earth ground shall not
Ground exceed 0.5 ohm.
Maximum Resistance Between PDU and Earth The resistance between the PDU ground and Earth ground shall not exceed 2
ohms.
Cable Shielding and Grounding All interconnect cables to peripheral devices shall be shielded and properly
grounded, except where technologically prohibited.
94 2 Grounding
3 System Interconnection and Cabling

3.1 Component Interconnections
The customer and electrical contractor shall refer to the following system, network, and power
interconnection requirements:
• Table 5-8 defines the component designators for system equipment, electrical components,
options, and communication outlets.
• Table 5-9 details the Standard-Length Cable Kit 5491000-3 (P5051TE) – Supplied by GE
Healthcare.
• Table 5-10 details the additional Standard-Length Cable Kit 5491000-10 (P5064TE) for 64-
slice systems – Supplied by GE Healthcare.
• Table 5-11 details the Long-Length Cable Kit, Optional 5491000-4 (P5051TF) – Supplied by
GE Healthcare.
• Table 5-12 details the additional Long-Length Cable Kit, Optional 5491000-20 (P5064TF) for
64-slice systems – Supplied by GE Healthcare.
• Table 5-13 details the PDU/UPS Cables (Standard-Length) – Supplied by GE Healthcare.
• Table 5-14 details the A1/UPS Cables – Supplied by GE Healthcare.
• Table 5-15 details the Miscellaneous Electrical Cables – Supplied by Customer/Contractor.
• Table 5-16 details the Miscellaneous Electrical Components – Supplied by Customer/

Contractor.
• Table 5-17 details the PARC4 (Q.Core Power) Upgrade Mandatory Cable Kit, Optional
5768790 (P3200ZH) for 64-slice systems – Supplied by GE Healthcare.
• Table 5-18 details the PARC4 (Q.Core Power) Upgrade Relocation Cable Kit, Optional
5768683 (P3200PT) for 64-slice systems – Supplied by GE Healthcare.
3.1.1 Component Designators

Table 5-8: Component Designators
Designator Applies to: Source
A1 Primary power disconnect Contractor-supplied
BBNC Broadband Network Connection Contractor-supplied
CT1 Patient Table System
CT2 Gantry System
DS Door Interlock Switch Contractor-supplied
OC1 Operator Console (Scanner Desktop)/computer System
PDU Power Distribution Unit System
PRC4 PARC4 (Q.Core Power) Reconstruction Cabinet System
SEO System Emergency Off Contractor-supplied
SM Slave Monitor Option

Designator Applies to: Source
WL X-ray ON warning light Contractor-supplied
3.1.2 Cable Specifications

Table 5-9: Standard-Length Cable Kit 5491000-3 (P5051TE) – Supplied by GE Healthcare
Run Length, Part Num‐ Description UL Cable Information Pull Size

# Actual ber mm (in.)
[Useable] UL Flame Volt‐ Actual Temp. Dia. mm # of Wire
m (ft) Style Rating age Volt‐ Rating (in.) Cond. Size
Rating age (C) (AWG)
PET Gantry to Console Cable Collector 5485380
56 25.5 5339979- Console GND 1238 VW-1 600 0 105 11.9 1 2 12.2 (0.5)
(83.7) 3 to Raceway (FT-1) (0.47)
[22.1 (73)] GND
102 26.4 2373436- Gantry to RG-2 FT-4 1900 <30 5.9 8 24 15 (0.6)
(86.6) 2 Console LAN 2 VDC (0.23)
[22.9 (75)]
101 26.4 5419981 Console to RG-2 FT-4 300 <30 80 11.2 25 22 17x58
(86.6) MSUB J9 2 VDC (0.44) (0.7x2.3)
[22.9 (75)] 19x51
(0.7x2.0)
103 25 (82) 2117848- Fiber Optic - NA NA 1 NA 10 (0.4)

Note [21.9 (72)] 2 Console to
1 Gantry (Not
Used)
XX 25 (82) 5432019 Fiber Optic - NA NA 1 NA

[21.9 (72)] (16 slice Gantry to
systems) Console
200 30.5 (100) 5313938- J7 to Console, UL FT-4 300 <30 60 6.8 4 pair 24 13 (0.5)
[22.9 (75)] 6 Respiratory VDC (0.26)
XX 28.2 5193969- Cable - LAN UL FT-4 60 24 40 (1.5)

(92.5) 4
[24.8 (82)]
XX 30.5 (100) 5169456 Gantry to In‐ 2464 FT-4 300 80 6.6 22 40 (1.5)
[27.7 (91)] jector (0.26)
XX 30.5 (100) 5199717 Gantry to UL FT-4 300 <15 5.9 4 22 15 (0.5)

[7.6 (25)] RPM Unit VDC (0.23)
PET Gantry to PDU Cable Collector 5485383
52A 8.6 (28.2) 2343528- PDU to Gan‐ 2587 FT-4 600 208Y/1 90 13.8 5 8 56.4 (2.2)
[6.1 (20)] 2 try 120VAC 20 (0.54)
52A 8.6 (28.2) 2343528- PDU to Gan‐ 2587 FT-4 600 208Y/1 90 13.8 5 8 56.4 (2.2)
Note [6.1 (20)] 4 try 120VAC 20 (0.54)
1 (Not Used)
50A 8.6 (28.2) 2343529- HVDC from 2587 FT-4 600 350 90 19 3 (2) 4, (1) 22 (0.9)
[6.1 (20)] 2 PDU to Gan‐ VDC (0.75) 8
try
51A 8.6 (28.2) 2343530- Axial Drive 2587 FT-4 600 440Y/2 90 12.3 4 14
[6.1 (20)] 2 Power PDU to 54 (0.48)
Gantry
96 3 System Interconnection and Cabling


55A 8.6 (28.2) 5339979- Raceway 1238 VW-1 600 0 105 11.9 1 2 12.2 (0.5)
[4.3 (14)] 2 GND to PDU - (FT-1) (0.47)
GND
100A 9.9 (32.5) 5120646- PDU to MSUB FT-4 300 <30 80 11.2 25 22 17x58
[6.1 (20)] 2 J11 VDC (0.44) (0.7x2.3)
19x51
(0.7x2.0)
PET Gantry to Q.Core Cable Collector 5485385
209A 13 (42.6) 5339979- Q.Core GND 1238 VW-1 600 0 105 11.9 1 2 12.2 (0.5)
[9.6 (32)] 6 to Raceway (FT-1) (0.47)
GND
203 13 (42.6) 5313938- SBA J7 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
[9.9 (33)] 7 Q.Core J6 VDC (0.26)
201 13 (42.6) 5313938- Q.Core J4 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
[8.4 (28)] 8 Switch Port 5 VDC (0.26)
202 13 (42.6) 5313938- PARC J5 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
Note [8.4 (28)] 9 Switch Port 7 VDC (0.26)
1 (Not Used)
Miscellaneous Cables in Kit 5491000-3
203 13 (42.6) 5313941– PDU TS5 to 2587 FT-4 600 208Y/1 60 19 5 10 25 (1.0)
Note [9.6 (32)] 2 PARC Bulk‐ 20 (0.75)
1 head (Not
Used)
203 13 (42.6) 2343531- Q.Core Power 2587 FT-4 600 120 90 11.7 3 10 56.4 (2.2)
[9.6 (32)] 4 from PDU, VAC (0.46)
short
053A 19.9 2343531- PDU TS5 to 2587 FT-4 600 120 90 12.2 3 10 56.4 (2.2)
(65.3) 2 Console Pow‐ VAC (0.48)
[16.6 (54)] er
Note 1: Extra Cable. Not used for Optima 560, Discovery 610, and Discovery 710 systems.
Table 5-10: Additional Standard-Length Cable Kit 5491000-10 (P5064TE) for 64-slice Systems
– Supplied by GE Healthcare

103 24.6 5125259 Fiber Optic - NA NA 1 NA

(80.7) Console to
[21.6 (71)] Gantry
053A 19.9 5121809- PDU TS5 to 2587 FT-4 600 208Y/1 90 12.3 4 10 56 (2.2)
Note (65.3) 2 Console Pow‐ 20 (0.48)
1 [16.6 (54)] er
Note 1: Not used. Extra cable (for GOC consoles only).

Table 5-11: Long-Length Cable Kit, Optional 5491000-4 (P5051TF) – Supplied by GE

Healthcare

m (ft) Style Rating age Voltage Rating (in.) Cond Size
Rating (C) . (AWG)
PET Gantry to Console Cable Collector 5485380
56 25.5 5339979-3 Console GND 1238 VW-1 600 0 105 11.9 1 2 12.2 (0.5)
(83.7) to Raceway (FT-1) (0.47)
[22.1 (73)] GND
102 26.4 2373436-2 Gantry to RG-2 FT-4 1900 <30 5.9 8 24 15 (0.6)
(86.6) Console LAN 2 VDC (0.23)
[22.9 (75)]
101 26.4 5419981 Console to RG-2 FT-4 300 <30 80 11.2 25 22 17x58
(86.6) MSUB J9 2 VDC (0.44) (0.7x2.3)
[22.9 (75)] 19x51
(0.7x2.0)
103 25 (82) 2117848-2 Fiber Optic - NA 1 NA 10 (0.4)

Note [21.9 (72)] Console to
1 Gantry (Not
Used)
XX 25 (82) 5432019 Fiber Optic - NA 1 NA

[21.9 (72)] (16 slice Gantry to
systems) Console
200 30.5 (100) 5313938-6 J7 to Con‐ UL FT-4 300 <30 60 6.8 4 pair 24 13 (0.5)
[22.9 (75)] sole, Respira‐ VDC (0.26)
tory
XX 28.2 5193969-4 Cable - LAN UL FT-4 60 24 40 (1.5)

(92.5)
[24.8 (82)]
XX 30.5 (100) 5169456 Gantry to In‐ 2464 FT-4 300 80 6.6 22 40 (1.5)
[27.7 (91)] jector (0.26)
XX 30.5 (100) 5199717 Gantry to UL FT-4 300 <15 5.9 4 22 15 (0.5)

[7.6 (25)] RPM Unit VDC (0.23)
PET Gantry to PDU Cable Collector 5485382
52 19.4 2343528 PDU to Gan‐ 2587 FT-4 600 208Y/1 90 13.8 5 8 56.4 (2.2)
(63.6) try 120VAC 20 (0.54)
[17.2 (56)]
52 19.4 2343528-3 PDU to Gan‐ 2587 FT-4 600 208Y/1 90 13.8 5 8 56.4 (2.2)
Note (63.6) try 120VAC 20 (0.54)
1 [17.2 (56)] (Not Used)
50 19.4 2343529 HVDC from 2587 FT-4 600 350 90 19 3 (2) 4, 22 (0.9)
(63.6) PDU to Gan‐ VDC (0.75) (1) 8
[17.2 (56)] try
51 19.4 2343530 Axial Drive 2587 FT-4 600 440Y/2 90 12.3 4 14

(63.6) Power PDU to 54 (0.48)
[17.2 (56)] Gantry
55 19.4 5339979 Raceway 1238 VW-1 600 0 105 11.9 1 2 12.2 (0.5)
(63.6) GND to PDU - (FT-1) (0.47)
[15.1 (50)] GND


m (ft) Style Rating age Voltage Rating (in.) Cond Size
Rating (C) . (AWG)
100 21.4 5120646 PDU to FT-4 300 <30 80 11.2 25 22 17x58

(70.2) MSUB J11 VDC (0.44) (0.7x2.3)
[18.9 (62)] 19x51
(0.7x2.0)
PET Gantry to Q.Core Cable Collector 5485384
209 25.5 5339979-5 Q.Core GND 1238 VW-1 600 0 105 11.9 (. 1 2 12.2 (0.5)
(83.6) to Raceway (FT-1) 47)
[22.1 (73)] GND
203 30.5 (100) 5313938 SBA J7 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
[27.4 (90)] Q.Core J6 VDC (0.26)
201 30.5 (100) 5313938-2 Q.Core J4 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
[25.9 (85)] Switch Port 5 VDC (0.26)
202 30.5 (100) 5313938-3 PARC J5 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
Note [25.9 (85)] Switch Port 7 VDC (0.26)
1 (Not Used)
Miscellaneous Cables in Kit 5491000-4
203 19.4 5313941 PDU TS5 to 2587 FT-4 600 208Y/1 60 19 5 10 25 (1.0)
Note (63.6) PARC Bulk‐ 20 (0.75)
1 [15.8 (52)] head (Not
Used)
203 19.4 2343531-3 Q.Core Power 2587 FT-4 600V 120 90 11.7 3 10 56.4 (2.2)
(63.6) [16 from PDU, VAC (0.46)
(52.6)] long
053 24.5 2343531 PDU TS5 to 2587 FT-4 600 120 90 12.3 3 10 56.4 (2.2)
(80.4) Console Pow‐ VAC (0.48)
[21.2 (69)] er
Note 1: Extra Cable. Not used for Optima 560, Discovery 610, and Discovery 710 systems.
Table 5-12: Additional Long-Length Cable Kit 5491000-20 (P5064TF) for 64-slice Systems –
Supplied by GE Healthcare

103 24.6 5125259 Fiber Optic - NA NA 1 NA

(80.7) Console to
[21.6 (71)] Gantry
053A 24.5 5121809 PDU TS5 to 2587 FT-4 600 208Y/1 90 12.3 4 10 56 (2.2)
Note (80.4) Console Pow‐ 20 (0.48)
1 [21.2 (69)] er
Note 1: Not used. Extra cable (for GOC consoles only).

Table 5-13: UPS Cables (Standard-Length) – Supplied by GE Healthcare
Run Cable Length, Part Descrip‐ UL Cable Information Pull Size

# Actual [Usa‐ Number tion mm (in.)
ble] m (ft) UL Flame Voltage Actual Temp. Dia. # of Wire
Style Rat‐ Rating Voltage Rating mm Cond. Size
ing (C) (in.) (AWG)
060 6 (19.7) [5 5125079 PDU to 2587 FT4 600 ± 350V 90 19 5 8 22 (0.9)

(16)] UPS DC (0.75) Dia.
061 6 (19.7) [5 5125079- UPS to 2587 FT4 600 440Y/ 90 15 5 8 22 (0.9)

(16)] 2 PDU 254 (0.60) Dia.
110 14 (46) [13.7 5169224 A1 to UPS 2587 FT4 600 208Y/ 90 14 5 18 25 (1.0)
(45)) 120 (0.54) Dia.
Table 5-14: A1 UPS
PDU Model No. Maximum Nomi‐ Required Mains Disconnect (A1) Catalog No. Optional Partial UPS Kit
nal kVA Rating Catalog No. (See Note 2)
Europe and Asia (380-400V or North America (440V or
420V) (See Note 1) 460-480V)
NGPDU-71 150 kVA E4502AF (150A) E4502AE (125A) B7864PZ

(64 slice systems) Includes Auto Restart and Inte‐ Includes Auto Restart and PowerWare 9355-15-
grated UPS Control Integrated UPS Control 14GE (14.4 kVa - 40A)
NGPDU-61 90 kVA E4502AC (110A) E4502AB (90A) B7864PZ

(16 slice systems) Includes Auto Restart and Inte‐ Includes Auto Restart and PowerWare 9355-15-
grated UPS Control Integrated UPS Control 14GE (14.4 kVa - 40A)
Note 1: Additional A1 Disconnects for Europe available through European Sales Team
Note 2: REQUIRES one of the A1 mains disconnect detailed at left, or equivalent.

Table 5-15: Miscellaneous Electrical Cables – Supplied by Customer/Contractor
Customer Installed Wiring Description Cables Supplied Plug Pulling Di‐ Wire and Cable Pig‐
mensions tails m (ft)
Qty Size AWG (mm2) Part No Length Dia. in. From To From To
m (ft) (mm)
RUN NO. 1 FROM PRIMARY POWER SOURCE TO FACILITY DISCONNECT (POWER SOURCE - A1)
Maximum Run Length *
3 * POWER 1 (3) 1 (3)
1 1/0 (50) GROUND 1 (3) 1 (3)
RUN NO. 2 FROM FACILITY DISCONNECT TO POWER DISTRIBUTION UNIT (A1 - PM)
Maximum Run Length *
3 * POWER 1 (3) 1 (3)
1 1/0 (50) GROUND 1 (3) 1 (3)
- - NEUTRAL - Not Required 1 (3) 1 (3)
RUN N0. 3 FROM FACILITY DISCONNECT TO SYSTEM EMERGENCY OFF (A1 - SEO)
2 14 (2) POWER 2 (6) 2 (6)
1 14 (2) GROUND 2 (6) 2 (6)
RUN NO. 4 POWER DISTRIBUTION UNIT TO WARNING LIGHT CONTROL (PDU - WL)
2 14 (2) WARNING LIGHT 24 VOLT
CONTROL TS6 1, 2, 3, 4, 5, 6,
7, 8
RUN NO. 5 POWER DISTRIBUTION UNIT TO SCAN ROOM DOOR INTERLOCK (PDU - DOOR SWITCH)
2 14 (2) SCAN ROOM DOOR INTER

LOCK TS6 9, 10
*REFER TO LOCAL BUILDING CODES FOR AWG (MM2) WIRE SIZES.
RUN NO. n/a BBNC
1 customer deter‐ Hospital Broadband Network

mined Connection (Wall Jack: Placed
on the wall behind the con‐
sole.)

Table 5-16: Miscellaneous Electrical Components – Supplied by Customer/Contractor
System Reference Associated Material/Labor Supplied by Customer USA Vendor / CAT No. GE Catalog
Equipment Contractor
64 Slice A1 Circuit Break‐ Three Pole, 380V - 480V, Combina‐ Recommend:

Discovery 610, 380V - 480V er with Mag‐ tion breaker with magnetic contactor. • E4502AE (125A)
Discovery 710 50/60 Hz netic Contac‐ Includes control transformer, optional
tor UPS interface, On/Off controls and au‐ • E4502AF (150A)
to-restart feature, if GE-supplied.
Optional remote operator control availa‐
ble from GE Supply, Cat #
GESCTR0CS1
16 Slice A1 Circuit Break‐ Three Pole, 200V - 240V or 380V - Recommend:

Optima 560, 200V - 240V, er with Mag‐ 480V, Combination breaker with mag‐ • E4502AC (110A)
Discovery 610, 380V - 480V netic Contac‐ netic contactor. Includes control trans‐
Discovery 710 50/60 Hz tor former, optional UPS interface, On/Off • E4502AB (90A)
controls and auto-restart feature, if
GE-supplied. Note: For systems with UPS, refer to Ta‐
ble 5-14 for A1 panel.
Optional remote operator control availa‐
ble from GE Supply, Cat #
GESCTR0CS1
All Systems BBNC (re‐ Broad-band Broad-Band network connection wall

quired) Network jack, located within 1m (39inches) of
Connection Operator Console location, for internal
hospital networking and InSite Broad-
Band connectivity. Cabling to conform
to facility’s IT standards.
All Systems System Com‐ Reference the system installation

ponents drawings supplied by Installation Sup‐
port Services within your geographic
area.
All Systems Room Warning Light Controller E4500AM
Table 5-17: PARC4 (Q.Core Power) Upgrade Mandatory Cable Kit 5768790 (P3200ZH) (64-
slice)

210 30.5 (100) 5313938- PARC J7 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
[22.9 (75)] 14 Switch J7, VDC (0.26)
Long
203 19.4 5313941 PDU-RRR 2587 FT-4 600 208Y/1 90 19 5 10 25 (1.0)

(63.6) POWER 20 (0.75)
[18.8
(61.7]

Table 5-18: PARC4 (Q.Core Power) Upgrade Relocation Cable Kit 5768683 (P3200PT) (64-
slice)
Length, Part Num‐ Description UL Cable Information Pull Size

Run Actual ber mm (in.)
# Style Rating age Volt‐ Rating (in.) Cond. Size
m (ft)
25.5 5339979- PARC GND to 1015, VW-1 600 0 105 11.9 (. 1 2 12.2 (0.5)
(83.6) 5 Raceway 1063, (FT-1) 47)
209
[21.8 GND Bar 1284,
(71.5)] 1283
30.5 (100) 5313938- RRR J4 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
201 [24.3 2 Switch Port 5 VDC (0.26)
(79.7)]
30.5 (100) 5313938 SBA J7 to UL FT-4 300 <30 60 6.6 4 pair 24 13 (0.5)
203
[27.4 (90)] RRR J6 VDC (0.26)
3.2 Cable Routing Requirements

3.2.1 Properly Sized Conduit, Duct Work, and Floor Troughs
Install appropriate conduits, duct work, and floor troughs for all system cables. Refer to Table
5-9 through Table 5-15.
NOTE: To minimize the need for additional junction boxes, use either a cable raceway
system or a raised computer floor. The system uses prefabricated cables with large
plugs.
3.2.2 Future Expansion
Ensure all cable passageways have additional capacity for future cable installations.
3.2.3 Routing Power Wiring
All three-phase power wires and ground line shall run in the same conduit or raceway duct.
3.2.4 Power and System Control Wire Separation
Power supply wires and system control lines shall be located in separate conduit or ductwork.

4 Scan Room Warning Light and Door Interlock

The scan room shall have a scan warning light and door interlock connected to the scan system
as detailed in the following diagrams.
4.1 X-Ray Warning Light
Illustration 5-3: TS6 X-Ray Warning Light Connections
A PDU 5 Line
B Facility supplied room light 6 Neutral
1 EXP_INTLK signal 7 X-RAY light
2 PGND 8 SYS-ON light
3 Fuse 9 READY light (Room Warning lamp)
4 24V secondary 10 Door Switch
4.2 Scan Room Door Interlock Connections

NOTE: The terminal blocks detailed in Illustration 5-4 and Illustration 5-5 are located in the
power distribution unit (PDU).
Illustration 5-4: TS6 Room Door Interlock Connections – without Door Interlock
104 4 Scan Room Warning Light and Door Interlock

Illustration 5-5: TS6 Room Door Interlock Connections – with Door Interlock
1 Normally open door switch

106 4 Scan Room Warning Light and Door Interlock

Chapter 6 Communications Requirements

1 Network Requirements
1.1 Communication Network
1.1.1 Network Wall Outlet
The customer shall provide an RJ45 wall outlet within 2 m (6.6 ft.) of the scanner desktop
location.
1.1.2 Network Speed
Broadband interface type: 10 Gb Ethernet connection.
1.1.3 Network Communication
The customer shall ensure a network broadband line is installed and active.
1.1.4 Patch Cable
The customer shall provide a patch cable, not to exceed 3.05 m (10 ft.), to connect the scanner
desktop to a wall outlet.
1.1.5 Cable Duct Work
The customer shall complete any cable duct work or conduit installation required for routing
network cables to workstation, camera, and scanner desktop.
1.1.6 Communication Run to RJ45 Wall Outlet
The customer shall ensure the communication run from the hospital/facility network switch to the
RJ45 wall outlet does not exceed 88 m (290 ft.).
1.2 Zone Broadband Specialist
1.2.1 Contact GE PM
Customer shall contact GE PM to obtain the name of a zone broadband specialist.
1.2.2 IT Infrastructure Changes
Zone broadband specialist will work with customer to complete identified infrastructure changes.
1.2.3 IP Addresses
Zone broadband specialist shall provide IP addresses for new system.
1.2.4 VPN Compatible Appliance
Zone broadband specialist shall provide a VPN compatible appliance to support the IPSec
tunneling protocol and 3DES data encryption.
1.2.5 Internet Service Provider
Zone broadband specialist shall utilize an Internet Service Provider that supports static routing.
Chapter 6 Communications Requirements 107

1.3 IT Site Contact Information

1.3.1 GE PM Information
Customer shall provide GE PM with an accurate site address, contact name, contact phone
number, and contact email address for customer IT person.
1.3.2 Coordinate VPN Activities
Site IT contact shall coordinate VPN activities between radiology/cardiology department and
Information Technology department.
1.3.3 Ensuring Broadband Infrastructure Requirements
Site IT contact will work as liaison to assure site broadband connectivity meets GE Healthcare
requirements, as determined by mutual assessment with GE Healthcare connectivity team.
1.3.4 Equipment Assessment
Site IT contact shall complete an equipment assessment with GE Healthcare connectivity team
to determine site broadband readiness.
108 1 Network Requirements

© 2017 General Electric Company. All Rights Reserved.
General Electric Company
3000 N. Grandview Boulevard
Waukesha, Wisconsin 53188
USA
www.gehealthcare.com

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Optima PET/CT 560, 560 FX; Discovery

PET/CT 610, 710

• Не използвайте оборудването, преди да сте се консултирали и разбрали

• Неспазването на това предупреждение може да доведе до нараняване на

UPOZORENJE Ovaj servisni priručnik dostupan je na engleskom jeziku.

VÝSTRAHA Tento provozní návod existuje pouze v anglickém jazyce.

• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního

ADVARSEL Denne servicemanual findes kun på engelsk.

• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.

• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk

WAARSCHUWING Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.

• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding

• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de

WARNING This service manual is available in English only.

HOIATUS See teenindusjuhend on saadaval ainult inglise keeles.

• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga

• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või pat‐

VAROITUS Tämä huolto-ohje on saatavilla vain englanniksi.

• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteis‐

ATTENTION Ce manuel d’installation et de maintenance est disponible uniquement en anglais.

• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur

WARNUNG Diese Serviceanleitung existiert nur in englischer Sprache.

• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendienst‐

ΠΡΟΕΙΔΟΠΟΙΗΣΗ Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.

• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός

FIGYELMEZTETÉS Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.

• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben

• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg

AÐVÖRUN Þessi þjónustuhandbók er aðeins fáanleg á ensku.

AVVERTENZA Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.

• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il pre‐

경고 본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다.

• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지

• 본 경고 사항에 유의하지 않으면 전기 쇼크, 기계적 위험, 또는 기타 위험으로 인해 서

BRĪDINĀJUMS Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.

• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un sapraša‐

• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, me‐

ĮSPĖJIMAS Šis eksploatavimo vadovas yra tik anglų kalba.

• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio

ADVARSEL Denne servicehåndboken finnes bare på engelsk.

• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.

OSTRZEŻENIE Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.

• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręczni‐

• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisan‐

ATENÇÃO Este manual de assistência técnica encontra-se disponível unicamente em inglês.

• A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou

ATENÇÃO Este manual de assistência técnica só se encontra disponível em inglês.

• O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do

ATENŢIE Acest manual de service este disponibil doar în limba engleză.

• Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui

• Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului

ОСТОРОЖНО! Данное руководство по техническому обслуживанию представлено только на

• Перед техническим обслуживанием оборудования обязательно обратитесь к

• Несоблюдение требований данного предупреждения может привести к тому,

UPOZORENJE Ovo servisno uputstvo je dostupno samo na engleskom jeziku.

• Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca

UPOZORNENIE Tento návod na obsluhu je k dispozícii len v angličtine.

• Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a nepor‐

• Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, ob‐

ATENCION Este manual de servicio sólo existe en inglés.

• No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido

VARNING Den här servicehandboken finns bara tillgänglig på engelska.

OPOZORILO Ta servisni priročnik je na voljo samo v angleškem jeziku.

• Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razu‐